Mutation

Primary Site >> Stomach Cancer

Gene >> BARHL2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370445
Start	90717087:90717087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.109G>A
AA Mutation	p.Glu37Lys(p.E37K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370445
Start	90714718:90714718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776330330
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Cys(p.R222C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370445
Start	90712473:90712473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003G>A
AA Mutation	p.Ala335Thr(p.A335T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370445
Start	90712453:90712453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1023G>A
AA Mutation	p.Met341Ile(p.M341I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370445
Start	90712562:90712562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764642090
CDS Mutation	c.914C>T
AA Mutation	p.Ser305Leu(p.S305L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370445
Start	90716915:90716915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538406922
CDS Mutation	c.281C>T
AA Mutation	p.Pro94Leu(p.P94L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370445
Start	90714725:90714725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370445
Start	90714575:90714575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370445
Start	90717013:90717013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370445
Start	90714605:90714605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.777G>A
Mutation Classification	Silent
Feature Type	Transcript