Colon Cancer: Gene >> DHRS9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357546
Start	169095735:169095735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.928A>G
AA Mutation	p.Lys310Glu(p.K310E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357546
Start	169083440:169083440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.425T>C
AA Mutation	p.Ile142Thr(p.I142T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357546
Start	169083366:169083366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770007864
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DHRS9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357546
Start	169095568:169095568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761A>C
AA Mutation	p.Lys254Thr(p.K254T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357546
Start	169091865:169091865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.648A>C
Mutation Classification	Silent
Feature Type	Transcript