Mutation

Primary Site >> Stomach Cancer

Gene >> WASF1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359451
Start	110127513:110127513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89C>T
AA Mutation	p.Thr30Ile(p.T30I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359451
Start	110107187:110107187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430G>T
AA Mutation	p.Gly144Cys(p.G144C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359451
Start	110103396:110103396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141943257
CDS Mutation	c.875C>T
AA Mutation	p.Pro292Leu(p.P292L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359451
Start	110103483:110103483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.788T>G
AA Mutation	p.Leu263Arg(p.L263R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359451
Start	110102170:110102170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940G>A
AA Mutation	p.Gly314Ser(p.G314S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359451
Start	110113347:110113347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247C>T
AA Mutation	p.Leu83Phe(p.L83F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359451
Start	110101841:110101841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567692835
CDS Mutation	c.1269G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359451
Start	110103515:110103515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359451
Start	110100597:110100597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1605G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000359451
Start	110102197:110102197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.913G>T
AA Mutation	p.Glu305Ter(p.E305*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript