Colon Cancer: Gene >> MTA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278823
Start	62596316:62596316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.979G>A
AA Mutation	p.Ala327Thr(p.A327T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278823
Start	62595270:62595270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1477G>A
AA Mutation	p.Ala493Thr(p.A493T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278823
Start	62594987:62594987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1567G>T
AA Mutation	p.Asp523Tyr(p.D523Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278823
Start	62600234:62600234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.122A>C
AA Mutation	p.Lys41Thr(p.K41T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278823
Start	62598374:62598374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325A>G
AA Mutation	p.Thr109Ala(p.T109A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000278823
Start	62598523:62598523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307C>T
AA Mutation	p.Arg103Trp(p.R103W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000278823
Start	62594406:62594406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1694T>C
AA Mutation	p.Met565Thr(p.M565T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000278823
Start	62594036:62594036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1846C>A
AA Mutation	p.Leu616Ile(p.L616I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000278823
Start	62594631:62594631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1577C>T
AA Mutation	p.Ala526Val(p.A526V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000278823
Start	62600217:62600217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Trp(p.R47W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000278823
Start	62598035:62598035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370573471
CDS Mutation	c.479G>A
AA Mutation	p.Arg160His(p.R160H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000278823
Start	62594032:62594032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1850G>A
AA Mutation	p.Arg617Gln(p.R617Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278823
Start	62594402:62594402(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1698delA
AA Mutation	p.Ala568GlnfsTer29(p.A568Qfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278823
Start	62598129:62598129(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.385delT
AA Mutation	p.Tyr129ThrfsTer33(p.Y129Tfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278823
Start	62594543:62594544(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1664dupG
AA Mutation	p.Ile556HisfsTer8(p.I556Hfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000278823
Start	62596108:62596108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MTA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278823
Start	62595479:62595479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268G>A
AA Mutation	p.Arg423Lys(p.R423K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278823
Start	62595431:62595431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1316C>G
AA Mutation	p.Thr439Ser(p.T439S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278823
Start	62594273:62594273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1827C>T
Mutation Classification	Silent
Feature Type	Transcript