Colon Cancer: Gene >> SRF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265354
Start	43178305:43178305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761821794
CDS Mutation	c.1174G>A
AA Mutation	p.Ala392Thr(p.A392T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265354
Start	43178459:43178459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1328T>C
AA Mutation	p.Val443Ala(p.V443A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265354
Start	43173988:43173988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655C>A
AA Mutation	p.Leu219Ile(p.L219I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265354
Start	43179167:43179167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1504G>A
AA Mutation	p.Ala502Thr(p.A502T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265354
Start	43175961:43175961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1036A>G
AA Mutation	p.Met346Val(p.M346V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265354
Start	43178319:43178319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537102728
CDS Mutation	c.1188G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SRF

No Mutation Annotation!