Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLC30A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000456015
Start	117157735:117157735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463A>T
AA Mutation	p.Thr155Ser(p.T155S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000456015
Start	117172562:117172562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991C>T
AA Mutation	p.Arg331Trp(p.R331W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000456015
Start	117146974:117146974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92C>A
AA Mutation	p.Pro31Gln(p.P31Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000456015
Start	117172662:117172662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1091G>T
AA Mutation	p.Cys364Phe(p.C364F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000456015
Start	117147073:117147073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774478941
CDS Mutation	c.191C>T
AA Mutation	p.Ala64Val(p.A64V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000456015
Start	117157694:117157694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.422T>C
AA Mutation	p.Ile141Thr(p.I141T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000456015
Start	117147068:117147068(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.190delG
AA Mutation	p.Ala64ArgfsTer22(p.A64Rfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000456015
Start	117147097:117147097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215G>A
AA Mutation	p.Trp72Ter(p.W72*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC30A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000456015
Start	117153064:117153064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778716564
CDS Mutation	c.392G>A
AA Mutation	p.Arg131Gln(p.R131Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000456015
Start	117171147:117171147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943C>A
AA Mutation	p.Leu315Ile(p.L315I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000456015
Start	117172596:117172596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1025T>G
AA Mutation	p.Phe342Cys(p.F342C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000456015
Start	117171086:117171086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768720476
CDS Mutation	c.882C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000456015
Start	117172609:117172609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1038A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000456015
Start	117157824:117157824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181713403
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript