Colon Cancer: Gene >> SOCS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330871
Start	78359014:78359014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82A>C
AA Mutation	p.Lys28Gln(p.K28Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330871
Start	78358815:78358815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.281G>A
AA Mutation	p.Arg94His(p.R94H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330871
Start	78358936:78358936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Gly54Ser(p.G54S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330871
Start	78358507:78358507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780147259
CDS Mutation	c.589G>A
AA Mutation	p.Val197Ile(p.V197I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330871
Start	78358643:78358643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371734270
CDS Mutation	c.453G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330871
Start	78358704:78358704(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.392delC
AA Mutation	p.Pro131LeufsTer48(p.P131Lfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330871
Start	78358797:78358797(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.299delG
AA Mutation	p.Gly100AlafsTer79(p.G100Afs*79)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SOCS3

No Mutation Annotation!