Colon Cancer: Gene >> SASH3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356892
Start	129792757:129792757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750800867
CDS Mutation	c.722G>A
AA Mutation	p.Arg241His(p.R241H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356892
Start	129792666:129792666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631G>T
AA Mutation	p.Gly211Cys(p.G211C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356892
Start	129792360:129792360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475G>A
AA Mutation	p.Gly159Ser(p.G159S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356892
Start	129793089:129793089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902A>G
AA Mutation	p.Gln301Arg(p.Q301R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356892
Start	129792472:129792472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587T>G
AA Mutation	p.Leu196Arg(p.L196R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356892
Start	129793726:129793726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037C>T
AA Mutation	p.Pro346Leu(p.P346L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356892
Start	129792734:129792734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768262427
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356892
Start	129793766:129793766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373319291
CDS Mutation	c.1077C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356892
Start	129791042:129791043(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.403_404insCATCCAC
AA Mutation	p.Glu135AlafsTer5(p.E135Afs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356892
Start	129792384:129792385(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.505dupC
AA Mutation	p.Gln169ProfsTer22(p.Q169Pfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000356892
Start	129793641:129793641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.953-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SASH3

No Mutation Annotation!