Colon Cancer: Gene >> NINL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25476919:25476919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141954162
CDS Mutation	c.2372C>T
AA Mutation	p.Ala791Val(p.A791V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25500936:25500936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.936C>A
AA Mutation	p.Phe312Leu(p.F312L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25512953:25512953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748131161
CDS Mutation	c.331C>T
AA Mutation	p.Arg111Cys(p.R111C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25526449:25526449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139G>A
AA Mutation	p.Val47Ile(p.V47I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25453504:25453504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4096C>T
AA Mutation	p.Arg1366Cys(p.R1366C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25476980:25476980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776042146
CDS Mutation	c.2311C>T
AA Mutation	p.Arg771Cys(p.R771C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25478950:25478950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2174G>T
AA Mutation	p.Arg725Leu(p.R725L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25476135:25476135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3156G>T
AA Mutation	p.Glu1052Asp(p.E1052D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25526428:25526428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200992599
CDS Mutation	c.160G>A
AA Mutation	p.Gly54Arg(p.G54R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25496763:25496763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1210A>G
AA Mutation	p.Arg404Gly(p.R404G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25504914:25504914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777310048
CDS Mutation	c.682G>A
AA Mutation	p.Val228Ile(p.V228I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25453621:25453621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3979G>A
AA Mutation	p.Asp1327Asn(p.D1327N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25504896:25504896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774911165
CDS Mutation	c.700G>A
AA Mutation	p.Glu234Lys(p.E234K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25479122:25479122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2002G>A
AA Mutation	p.Glu668Lys(p.E668K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25462399:25462399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3566G>T
AA Mutation	p.Arg1189Leu(p.R1189L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25479125:25479125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750950764
CDS Mutation	c.1999C>T
AA Mutation	p.Arg667Cys(p.R667C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25476346:25476346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2945G>A
AA Mutation	p.Arg982Gln(p.R982Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25491485:25491485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375539708
CDS Mutation	c.1351C>T
AA Mutation	p.Arg451Trp(p.R451W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25479181:25479181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141944908
CDS Mutation	c.1943C>T
AA Mutation	p.Ala648Val(p.A648V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25505041:25505041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532756641
CDS Mutation	c.555C>G
AA Mutation	p.Ser185Arg(p.S185R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278886
Start	25489280:25489280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148450519
CDS Mutation	c.1641C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278886
Start	25526423:25526423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374578020
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278886
Start	25476591:25476591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758746224
CDS Mutation	c.2700C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278886
Start	25489981:25489981(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1490delA
AA Mutation	p.Asn497ThrfsTer23(p.N497Tfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000278886
Start	25478982:25478982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2142C>A
AA Mutation	p.Cys714Ter(p.C714*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278886
Start	25461617:25461618(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3600dupA
AA Mutation	p.Leu1201ThrfsTer2(p.L1201Tfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278886
Start	25500969:25500970(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.902_903insAG
AA Mutation	p.Leu302AlafsTer54(p.L302Afs*54)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NINL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25504896:25504896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774911165
CDS Mutation	c.700G>A
AA Mutation	p.Glu234Lys(p.E234K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25477075:25477075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757912343
CDS Mutation	c.2216C>T
AA Mutation	p.Ala739Val(p.A739V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25455750:25455750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759311453
CDS Mutation	c.3880C>T
AA Mutation	p.Arg1294Trp(p.R1294W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25504914:25504914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777310048
CDS Mutation	c.682G>A
AA Mutation	p.Val228Ile(p.V228I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25462400:25462400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781248065
CDS Mutation	c.3565C>T
AA Mutation	p.Arg1189Cys(p.R1189C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25476889:25476889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2402C>T
AA Mutation	p.Ser801Leu(p.S801L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000278886
Start	25489930:25489930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1541C>T
AA Mutation	p.Ser514Leu(p.S514L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278886
Start	25476816:25476816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2475G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278886
Start	25512948:25512948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.336G>T
Mutation Classification	Silent
Feature Type	Transcript