Mutation

Primary Site >> Stomach Cancer

Gene >> SLC4A2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000413384
Start	151071751:151071751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139758611
CDS Mutation	c.2254G>A
AA Mutation	p.Val752Met(p.V752M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000413384
Start	151074291:151074291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777711244
CDS Mutation	c.2788C>T
AA Mutation	p.Arg930Trp(p.R930W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000413384
Start	151067925:151067925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018T>A
AA Mutation	p.Trp340Arg(p.W340R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000413384
Start	151071150:151071150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781096714
CDS Mutation	c.1828G>A
AA Mutation	p.Val610Met(p.V610M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000413384
Start	151071434:151071434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2020C>T
AA Mutation	p.Pro674Ser(p.P674S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000413384
Start	151075482:151075482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370805035
CDS Mutation	c.3275C>T
AA Mutation	p.Thr1092Met(p.T1092M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000413384
Start	151074259:151074259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2756G>A
AA Mutation	p.Arg919His(p.R919H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000413384
Start	151064335:151064335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.185C>T
AA Mutation	p.Pro62Leu(p.P62L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000413384
Start	151075736:151075736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3432G>A
AA Mutation	p.Met1144Ile(p.M1144I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000413384
Start	151075298:151075298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376108278
CDS Mutation	c.3091G>A
AA Mutation	p.Gly1031Ser(p.G1031S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000413384
Start	151070765:151070765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1603G>A
AA Mutation	p.Val535Met(p.V535M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000413384
Start	151064649:151064649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341C>A
AA Mutation	p.Pro114Gln(p.P114Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000413384
Start	151064310:151064310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160G>T
AA Mutation	p.Ala54Ser(p.A54S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000413384
Start	151074701:151074701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17852574
CDS Mutation	c.2907G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000413384
Start	151061996:151061996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000413384
Start	151075405:151075405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3198C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000413384
Start	151064677:151064677(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.373delG
AA Mutation	p.Glu125ArgfsTer120(p.E125Rfs*120)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000413384
Start	151074736:151074737(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2947dupC
AA Mutation	p.Leu983ProfsTer149(p.L983Pfs*149)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	19
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000413384
Start	151074490:151074490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2880+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript