Mutation

Primary Site >> Stomach Cancer

Gene >> SLC4A1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262418
Start	44253130:44253130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2299G>T
AA Mutation	p.Ala767Ser(p.A767S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262418
Start	44253327:44253327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121912748
CDS Mutation	c.2102G>A
AA Mutation	p.Gly701Asp(p.G701D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262418
Start	44260452:44260452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777835021
CDS Mutation	c.437G>A
AA Mutation	p.Arg146Gln(p.R146Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262418
Start	44260751:44260751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186542577
CDS Mutation	c.233C>T
AA Mutation	p.Ala78Val(p.A78V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262418
Start	44260748:44260748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376688172
CDS Mutation	c.236C>T
AA Mutation	p.Ala79Val(p.A79V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262418
Start	44258105:44258105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760404726
CDS Mutation	c.1163G>A
AA Mutation	p.Arg388His(p.R388H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262418
Start	44253348:44253348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745505408
CDS Mutation	c.2081G>A
AA Mutation	p.Arg694His(p.R694H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262418
Start	44258109:44258109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531459694
CDS Mutation	c.1159C>T
AA Mutation	p.Arg387Trp(p.R387W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262418
Start	44251265:44251265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2549T>C
AA Mutation	p.Val850Ala(p.V850A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262418
Start	44257514:44257514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28931584
CDS Mutation	c.1462G>A
AA Mutation	p.Val488Met(p.V488M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262418
Start	44261590:44261590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153C>A
AA Mutation	p.His51Gln(p.H51Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262418
Start	44258464:44258464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371106409
CDS Mutation	c.1036C>T
AA Mutation	p.Arg346Cys(p.R346C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262418
Start	44262661:44262661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771695604
CDS Mutation	c.81C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262418
Start	44257530:44257530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367899879
CDS Mutation	c.1446C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262418
Start	44259903:44259903(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.515delG
AA Mutation	p.Gly172ValfsTer2(p.G172Vfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262418
Start	44259216:44259216(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.823delC
AA Mutation	p.His275ThrfsTer22(p.H275Tfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262418
Start	44259902:44259903(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.515dupG
AA Mutation	p.Val173CysfsTer30(p.V173Cfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript