Colon Cancer: Gene >> SLC16A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369779
Start	110389313:110389313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754334971
CDS Mutation	c.11G>A
AA Mutation	p.Arg4Lys(p.R4K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369779
Start	110379237:110379237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646T>C
AA Mutation	p.Ser216Pro(p.S216P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369779
Start	110377005:110377005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1187C>A
AA Mutation	p.Thr396Asn(p.T396N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000369779
Start	110380980:110380980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SLC16A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369779
Start	110381080:110381080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428G>A
AA Mutation	p.Arg143Gln(p.R143Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369779
Start	110379115:110379115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.768A>C
AA Mutation	p.Gln256His(p.Q256H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript