Colon Cancer: Gene >> TNFRSF10C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356864
Start	23116718:23116718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376360379
CDS Mutation	c.467A>G
AA Mutation	p.Asn156Ser(p.N156S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356864
Start	23115604:23115604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755521340
CDS Mutation	c.377G>A
AA Mutation	p.Arg126Gln(p.R126Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356864
Start	23114738:23114738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248C>T
AA Mutation	p.Pro83Leu(p.P83L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356864
Start	23111806:23111806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147G>T
AA Mutation	p.Lys49Asn(p.K49N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356864
Start	23114751:23114751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF10C

No Mutation Annotation!