Mutation

Primary Site >> Stomach Cancer

Gene >> SLC22A16

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110431259:110431259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1433T>C
AA Mutation	p.Val478Ala(p.V478A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110438755:110438755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1276G>T
AA Mutation	p.Ala426Ser(p.A426S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110425060:110425060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547T>G
AA Mutation	p.Leu516Arg(p.L516R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110456866:110456866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.205T>C
AA Mutation	p.Trp69Arg(p.W69R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110425067:110425067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1540G>A
AA Mutation	p.Ala514Thr(p.A514T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110442498:110442498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929T>C
AA Mutation	p.Ile310Thr(p.I310T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110438826:110438826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1205A>G
AA Mutation	p.Tyr402Cys(p.Y402C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110456718:110456718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353G>A
AA Mutation	p.Gly118Asp(p.G118D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110424907:110424907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770486939
CDS Mutation	c.1700C>T
AA Mutation	p.Ala567Val(p.A567V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110456760:110456760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311A>C
AA Mutation	p.Asn104Thr(p.N104T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368919
Start	110442386:110442386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1041A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368919
Start	110442508:110442508(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.919delA
AA Mutation	p.Ile307Ter(p.I307*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368919
Start	110424914:110424914(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1693delA
AA Mutation	p.Thr565ArgfsTer21(p.T565Rfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript