Colon Cancer: Gene >> MLXIPL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313375
Start	73596386:73596386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781908299
CDS Mutation	c.1916G>A
AA Mutation	p.Arg639Gln(p.R639Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313375
Start	73599563:73599563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551026243
CDS Mutation	c.1034C>T
AA Mutation	p.Ser345Leu(p.S345L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313375
Start	73597470:73597470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315A>G
AA Mutation	p.Thr439Ala(p.T439A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313375
Start	73597526:73597526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1259C>A
AA Mutation	p.Pro420Gln(p.P420Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313375
Start	73607386:73607386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518G>A
AA Mutation	p.Arg173His(p.R173H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313375
Start	73624294:73624294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199G>C
AA Mutation	p.Asp67His(p.D67H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313375
Start	73594287:73594287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370106365
CDS Mutation	c.2427C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313375
Start	73624271:73624271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MLXIPL

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313375
Start	73597468:73597468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1317C>T
Mutation Classification	Silent
Feature Type	Transcript