Colon Cancer: Gene >> SLC26A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286298
Start	149977910:149977910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258A>T
AA Mutation	p.Lys86Asn(p.K86N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286298
Start	149978224:149978224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763693887
CDS Mutation	c.572C>T
AA Mutation	p.Ala191Val(p.A191V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286298
Start	149980479:149980479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.886A>G
AA Mutation	p.Asn296Asp(p.N296D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286298
Start	149981754:149981754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2161G>A
AA Mutation	p.Val721Ile(p.V721I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286298
Start	149980851:149980851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1258G>A
AA Mutation	p.Ala420Thr(p.A420T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000286298
Start	149977783:149977783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131C>T
AA Mutation	p.Thr44Ile(p.T44I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000286298
Start	149980515:149980515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922A>C
AA Mutation	p.Ser308Arg(p.S308R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000286298
Start	149980628:149980628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1035A>T
AA Mutation	p.Leu345Phe(p.L345F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286298
Start	149980859:149980859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1266C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286298
Start	149981537:149981537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1944T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286298
Start	149981681:149981681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780668685
CDS Mutation	c.2088C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000286298
Start	149980653:149980653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1060G>T
AA Mutation	p.Glu354Ter(p.E354*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC26A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286298
Start	149980731:149980731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138C>T
AA Mutation	p.Pro380Ser(p.P380S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286298
Start	149981449:149981449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1856G>T
AA Mutation	p.Arg619Ile(p.R619I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286298
Start	149981200:149981200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1607G>T
AA Mutation	p.Cys536Phe(p.C536F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286298
Start	149977832:149977832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180G>T
AA Mutation	p.Glu60Asp(p.E60D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286298
Start	149978132:149978132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.480C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286298
Start	149977688:149977688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.36A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000286298
Start	149980551:149980551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958G>T
AA Mutation	p.Glu320Ter(p.E320*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript