Colon Cancer: Gene >> SLC25A20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319017
Start	48859103:48859103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.707G>A
AA Mutation	p.Arg236Gln(p.R236Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319017
Start	48879411:48879411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150419695
CDS Mutation	c.364G>A
AA Mutation	p.Val122Ile(p.V122I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319017
Start	48892008:48892008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170A>G
AA Mutation	p.Asp57Gly(p.D57G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319017
Start	48862588:48862588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000319017
Start	48879399:48879399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376G>T
AA Mutation	p.Gly126Ter(p.G126*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319017
Start	48891995:48891995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183G>T
AA Mutation	p.Lys61Asn(p.K61N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319017
Start	48862585:48862585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492G>C
Mutation Classification	Silent
Feature Type	Transcript