Mutation

Primary Site >> Stomach Cancer

Gene >> COL11A1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102914763:102914763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3865G>T
AA Mutation	p.Ala1289Ser(p.A1289S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370096
Start	102883309:102883309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4861G>A
AA Mutation	p.Glu1621Lys(p.E1621K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	103014520:103014520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563G>T
AA Mutation	p.Gln521His(p.Q521H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102984184:102984184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2510T>A
AA Mutation	p.Leu837His(p.L837H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102878078:102878078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5362T>C
AA Mutation	p.Phe1788Leu(p.F1788L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	103074626:103074626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643G>T
AA Mutation	p.Val215Phe(p.V215F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	103074627:103074627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.642A>C
AA Mutation	p.Glu214Asp(p.E214D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	103108114:103108114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.65T>C
AA Mutation	p.Leu22Pro(p.L22P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102879868:102879868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5089A>G
AA Mutation	p.Thr1697Ala(p.T1697A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102923383:102923383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3607C>T
AA Mutation	p.Pro1203Ser(p.P1203S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102879832:102879832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5125A>C
AA Mutation	p.Asn1709His(p.N1709H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102889550:102889550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4369T>G
AA Mutation	p.Leu1457Val(p.L1457V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102946875:102946875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3250G>A
AA Mutation	p.Gly1084Ser(p.G1084S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	103082940:103082940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139T>C
AA Mutation	p.Phe47Leu(p.F47L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	103082961:103082961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.118G>A
AA Mutation	p.Asp40Asn(p.D40N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	103012448:103012448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1594G>T
AA Mutation	p.Gly532Cys(p.G532C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102984184:102984184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2510T>G
AA Mutation	p.Leu837Arg(p.L837R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102962190:102962190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3100C>T
AA Mutation	p.Leu1034Phe(p.L1034F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102962662:102962662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3015A>T
AA Mutation	p.Glu1005Asp(p.E1005D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102984184:102984184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2510T>C
AA Mutation	p.Leu837Pro(p.L837P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102921525:102921525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3701G>A
AA Mutation	p.Gly1234Glu(p.G1234E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102987640:102987640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2495G>A
AA Mutation	p.Gly832Glu(p.G832E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102996023:102996023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2261G>T
AA Mutation	p.Gly754Val(p.G754V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	103022905:103022905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372451206
CDS Mutation	c.1082A>G
AA Mutation	p.Glu361Gly(p.E361G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102889477:102889477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4442C>G
AA Mutation	p.Ser1481Cys(p.S1481C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102878078:102878078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571497194
CDS Mutation	c.5362T>G
AA Mutation	p.Phe1788Val(p.F1788V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	103108145:103108145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34C>T
AA Mutation	p.Arg12Trp(p.R12W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102886969:102886969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780611200
CDS Mutation	c.4696G>T
AA Mutation	p.Asp1566Tyr(p.D1566Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102920348:102920348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3725C>A
AA Mutation	p.Pro1242Gln(p.P1242Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102962681:102962681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2996C>T
AA Mutation	p.Pro999Leu(p.P999L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	103008510:103008510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777447423
CDS Mutation	c.1636C>G
AA Mutation	p.Pro546Ala(p.P546A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102879829:102879829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5128T>G
AA Mutation	p.Phe1710Val(p.F1710V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102879828:102879828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5129T>C
AA Mutation	p.Phe1710Ser(p.F1710S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102962676:102962676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3001G>T
AA Mutation	p.Ala1001Ser(p.A1001S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102970224:102970224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2857G>A
AA Mutation	p.Glu953Lys(p.E953K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102887023:102887023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4642A>T
AA Mutation	p.Ile1548Phe(p.I1548F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000370096
Start	102886971:102886971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4694C>T
AA Mutation	p.Ala1565Val(p.A1565V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	103025596:103025596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.915T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	103074708:103074708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368813913
CDS Mutation	c.561G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	102913643:102913643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4026T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	102978878:102978878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2691T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	102878139:102878139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5301C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	102914400:102914400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3930T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	102987699:102987699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2436T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	103022754:103022754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	103078813:103078813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	102888747:102888747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775945644
CDS Mutation	c.4530C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	102984174:102984174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2520A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	102921521:102921521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3705T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	50
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	102961914:102961914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3120A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	102962245:102962245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3045T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	52
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370096
Start	102920359:102920359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3714A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	53
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370096
Start	103008511:103008511(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1635delG
AA Mutation	p.Pro546LeufsTer87(p.P546Lfs*87)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	54
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370096
Start	103015735:103015735(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1421delC
AA Mutation	p.Pro474GlnfsTer20(p.P474Qfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	55
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370096
Start	102887005:102887005(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4660delA
AA Mutation	p.Thr1554ArgfsTer33(p.T1554Rfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	56
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370096
Start	102889507:102889507(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4412delG
AA Mutation	p.Gly1471ValfsTer27(p.G1471Vfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	57
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370096
Start	103082950:103082950(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.129delA
AA Mutation	p.Ala44HisfsTer2(p.A44Hfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	58
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000370096
Start	102920312:102920312(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3761delA
AA Mutation	p.Lys1254ArgfsTer18(p.K1254Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	59
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370096
Start	102898950:102898950(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4131delA
AA Mutation	p.Gly1378ValfsTer80(p.G1378Vfs*80)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	60
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370096
Start	102898770:102898770(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4144delG
AA Mutation	p.Glu1382LysfsTer76(p.E1382Kfs*76)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	61
Mutation Consequence	stop_gained
Transcription ID	ENST00000370096
Start	103004470:103004470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1918G>T
AA Mutation	p.Gly640Ter(p.G640*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	62
Mutation Consequence	stop_gained
Transcription ID	ENST00000370096
Start	103082856:103082856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.223A>T
AA Mutation	p.Arg75Ter(p.R75*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	63
Mutation Consequence	stop_gained
Transcription ID	ENST00000370096
Start	103005885:103005885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1798C>T
AA Mutation	p.Arg600Ter(p.R600*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	64
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000370096
Start	102888721:102888721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4554+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	65
Mutation Consequence	stop_lost
Transcription ID	ENST00000370096
Start	102878019:102878019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5421A>C
AA Mutation	p.Ter1807TyrextTer2(p.1807Yext2)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript