Colon Cancer: Gene >> TNFSF15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374045
Start	114790777:114790777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368084272
CDS Mutation	c.431C>T
AA Mutation	p.Ser144Leu(p.S144L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374045
Start	114790612:114790612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.596A>C
AA Mutation	p.Lys199Thr(p.K199T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374045
Start	114790789:114790789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419T>G
AA Mutation	p.Leu140Arg(p.L140R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374045
Start	114790521:114790521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754459102
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374045
Start	114790602:114790602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184980312
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374045
Start	114790623:114790623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000374045
Start	114793532:114793532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.247C>T
AA Mutation	p.Gln83Ter(p.Q83*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TNFSF15

No Mutation Annotation!