Colon Cancer: Gene >> SDR9C7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293502
Start	56929395:56929395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374904822
CDS Mutation	c.719G>A
AA Mutation	p.Arg240His(p.R240H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293502
Start	56930371:56930371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142269600
CDS Mutation	c.415G>A
AA Mutation	p.Glu139Lys(p.E139K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293502
Start	56933967:56933967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374817950
CDS Mutation	c.295G>A
AA Mutation	p.Glu99Lys(p.E99K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000293502
Start	56929551:56929551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141626978
CDS Mutation	c.563G>A
AA Mutation	p.Arg188His(p.R188H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000293502
Start	56934222:56934222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40T>C
AA Mutation	p.Phe14Leu(p.F14L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293502
Start	56933968:56933968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750869501
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293502
Start	56930267:56930267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139321947
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SDR9C7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293502
Start	56934048:56934048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530109812
CDS Mutation	c.214C>T
AA Mutation	p.Arg72Trp(p.R72W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript