Mutation

Primary Site >> Stomach Cancer

Gene >> SH2D3C

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314830
Start	127744793:127744793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1571G>T
AA Mutation	p.Arg524Met(p.R524M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314830
Start	127744766:127744766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1598C>T
AA Mutation	p.Ala533Val(p.A533V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314830
Start	127744598:127744598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571887895
CDS Mutation	c.1766C>T
AA Mutation	p.Thr589Met(p.T589M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314830
Start	127774329:127774329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781633475
CDS Mutation	c.176C>T
AA Mutation	p.Thr59Met(p.T59M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000314830
Start	127744583:127744583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538164583
CDS Mutation	c.1781T>C
AA Mutation	p.Val594Ala(p.V594A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314830
Start	127741806:127741806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2070T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314830
Start	127774463:127774463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314830
Start	127741896:127741896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1980G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314830
Start	127739812:127739812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2277A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314830
Start	127774328:127774328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533827308
CDS Mutation	c.177G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000314830
Start	127744848:127744848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1516C>T
AA Mutation	p.Arg506Ter(p.R506*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000314830
Start	127740346:127740346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2112G>A
AA Mutation	p.Trp704Ter(p.W704*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314830
Start	127744993:127744994(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1370dupC
AA Mutation	p.Thr459AspfsTer31(p.T459Dfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript