Colon Cancer: Gene >> TOR1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259339
Start	129804142:129804142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.269T>C
AA Mutation	p.Leu90Pro(p.L90P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259339
Start	129809011:129809011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774583128
CDS Mutation	c.748G>A
AA Mutation	p.Gly250Arg(p.G250R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000259339
Start	129807362:129807362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.640A>G
AA Mutation	p.Ser214Gly(p.S214G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259339
Start	129809384:129809384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.812A>C
AA Mutation	p.Asp271Ala(p.D271A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000259339
Start	129809368:129809368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777793156
CDS Mutation	c.796G>A
AA Mutation	p.Asp266Asn(p.D266N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000259339
Start	129809480:129809480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.908T>C
AA Mutation	p.Ile303Thr(p.I303T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TOR1B

No Mutation Annotation!