Colon Cancer: Gene >> S100G

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000380200
Start	16654406:16654406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137G>T
AA Mutation	p.Gly46Val(p.G46V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380200
Start	16651043:16651043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37A>T
AA Mutation	p.Ile13Phe(p.I13F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380200
Start	16651076:16651076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70C>A
AA Mutation	p.Pro24Thr(p.P24T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380200
Start	16654458:16654458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.189A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> S100G

No Mutation Annotation!