Colon Cancer: Gene >> VPS41

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310301
Start	38771221:38771221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162A>T
AA Mutation	p.Asn388Tyr(p.N388Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310301
Start	38795607:38795607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.575T>C
AA Mutation	p.Val192Ala(p.V192A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310301
Start	38756918:38756918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760327026
CDS Mutation	c.1615G>A
AA Mutation	p.Val539Ile(p.V539I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310301
Start	38763502:38763502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1375C>T
AA Mutation	p.Leu459Phe(p.L459F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310301
Start	38772567:38772567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1083C>A
AA Mutation	p.Asp361Glu(p.D361E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310301
Start	38752285:38752285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1817A>G
AA Mutation	p.His606Arg(p.H606R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310301
Start	38742058:38742058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2186G>A
AA Mutation	p.Arg729His(p.R729H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000310301
Start	38776707:38776707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854C>T
AA Mutation	p.Ser285Leu(p.S285L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000310301
Start	38758412:38758412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1492C>T
AA Mutation	p.Arg498Trp(p.R498W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310301
Start	38728771:38728771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2280C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310301
Start	38742005:38742005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2239C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310301
Start	38756883:38756883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1650T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310301
Start	38756919:38756919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146405914
CDS Mutation	c.1614C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310301
Start	38817859:38817859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150900239
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310301
Start	38771220:38771220(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs757692785
CDS Mutation	c.1163delA
AA Mutation	p.Asn388IlefsTer15(p.N388Ifs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000310301
Start	38752274:38752274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1828C>T
AA Mutation	p.Gln610Ter(p.Q610*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000310301
Start	38776680:38776681(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.880dupA
AA Mutation	p.Thr294AsnfsTer10(p.T294Nfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> VPS41

No Mutation Annotation!