Colon Cancer: Gene >> GDF11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257868
Start	55749778:55749778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120C>A
AA Mutation	p.Pro374Thr(p.P374T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257868
Start	55748697:55748697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.557C>T
AA Mutation	p.Pro186Leu(p.P186L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257868
Start	55748789:55748789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649C>T
AA Mutation	p.Arg217Cys(p.R217C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257868
Start	55749835:55749835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177T>C
AA Mutation	p.Tyr393His(p.Y393H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257868
Start	55749745:55749745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087A>T
AA Mutation	p.Asn363Tyr(p.N363Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257868
Start	55749747:55749747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1089T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257868
Start	55749633:55749633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.975C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GDF11

No Mutation Annotation!