Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PIK3C2G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18343352:18343352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1421C>T
AA Mutation	p.Ser474Leu(p.S474L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18282310:18282310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.229T>G
AA Mutation	p.Ser77Ala(p.S77A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18538257:18538257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774205366
CDS Mutation	c.3302G>A
AA Mutation	p.Arg1101His(p.R1101H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000266497
Start	18338426:18338426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1273G>A
AA Mutation	p.Glu425Lys(p.E425K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18496074:18496074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2683T>G
AA Mutation	p.Phe895Val(p.F895V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18497634:18497634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368805708
CDS Mutation	c.2779C>T
AA Mutation	p.Arg927Cys(p.R927C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18381848:18381848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764184362
CDS Mutation	c.1840G>A
AA Mutation	p.Asp614Asn(p.D614N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18338465:18338465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1312T>C
AA Mutation	p.Cys438Arg(p.C438R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18538297:18538297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3342G>T
AA Mutation	p.Leu1114Phe(p.L1114F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18546392:18546392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3427C>G
AA Mutation	p.Pro1143Ala(p.P1143A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18282154:18282154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777959749
CDS Mutation	c.73C>A
AA Mutation	p.Leu25Ile(p.L25I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18282416:18282416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.335C>T
AA Mutation	p.Ser112Phe(p.S112F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18609577:18609577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4007T>C
AA Mutation	p.Ile1336Thr(p.I1336T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266497
Start	18647989:18647989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4299T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266497
Start	18314028:18314028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1101G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266497
Start	18562760:18562760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3525A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266497
Start	18538301:18538301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3346C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266497
Start	18282366:18282366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266497
Start	18488455:18488455(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2393delA
AA Mutation	p.Asn798MetfsTer16(p.N798Mfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266497
Start	18338456:18338456(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1309delA
AA Mutation	p.Ile437TyrfsTer5(p.I437Yfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000266497
Start	18648011:18648011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4321G>T
AA Mutation	p.Gly1441Ter(p.G1441*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000266497
Start	18282148:18282148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67G>T
AA Mutation	p.Glu23Ter(p.E23*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000266497
Start	18282649:18282649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568G>T
AA Mutation	p.Glu190Ter(p.E190*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000266497
Start	18647993:18647993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4303G>T
AA Mutation	p.Glu1435Ter(p.E1435*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000266497
Start	18294002:18294002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377755015
CDS Mutation	c.1021G>T
AA Mutation	p.Glu341Ter(p.E341*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000266497
Start	18282122:18282122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41C>G
AA Mutation	p.Ser14Ter(p.S14*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000266497
Start	18290870:18290870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.777T>G
AA Mutation	p.Tyr259Ter(p.Y259*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000266497
Start	18594548:18594548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3943G>T
AA Mutation	p.Glu1315Ter(p.E1315*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266497
Start	18282267:18282268(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.192dupT
AA Mutation	p.Val65CysfsTer16(p.V65Cfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266497
Start	18648001:18648002(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4311_4312insCTAA
AA Mutation	p.Tyr1438LeufsTer21(p.Y1438Lfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000266497
Start	18562746:18562754(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3511_3519delAACTTGATC
AA Mutation	p.Asn1171_Ile1173del(p.N1171_I1173del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PIK3C2G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18609546:18609546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3976C>A
AA Mutation	p.Pro1326Thr(p.P1326T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18505340:18505340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3079T>C
AA Mutation	p.Phe1027Leu(p.F1027L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18290971:18290971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878T>G
AA Mutation	p.Phe293Cys(p.F293C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18497650:18497650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs387907453
CDS Mutation	c.2795T>C
AA Mutation	p.Val932Ala(p.V932A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18566980:18566980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3811A>G
AA Mutation	p.Asn1271Asp(p.N1271D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266497
Start	18609624:18609624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4054A>T
AA Mutation	p.Asn1352Tyr(p.N1352Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266497
Start	18282267:18282267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266497
Start	18282168:18282168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.87A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266497
Start	18488455:18488455(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2393delA
AA Mutation	p.Asn798MetfsTer16(p.N798Mfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript