Colon Cancer: Gene >> ATP1B2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250111
Start	7655849:7655849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.827A>G
AA Mutation	p.Lys276Arg(p.K276R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250111
Start	7653476:7653476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215A>C
AA Mutation	p.Lys72Thr(p.K72T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250111
Start	7655861:7655861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765289769
CDS Mutation	c.839G>A
AA Mutation	p.Arg280His(p.R280H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000250111
Start	7653945:7653945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346C>T
AA Mutation	p.Pro116Ser(p.P116S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000250111
Start	7653488:7653488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755969286
CDS Mutation	c.227G>A
AA Mutation	p.Arg76Gln(p.R76Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250111
Start	7655793:7655793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250111
Start	7654140:7654140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250111
Start	7655856:7655856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377624994
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250111
Start	7653398:7653398(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.142delT
AA Mutation	p.Tyr48MetfsTer14(p.Y48Mfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250111
Start	7654144:7654144(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.441delA
AA Mutation	p.Lys147AsnfsTer36(p.K147Nfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ATP1B2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250111
Start	7653938:7653938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339C>A
AA Mutation	p.Phe113Leu(p.F113L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250111
Start	7655616:7655616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699A>C
AA Mutation	p.Lys233Asn(p.K233N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript