Colon Cancer: Gene >> HDAC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48824178:48824178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782674799
CDS Mutation	c.3463C>T
AA Mutation	p.Arg1155Cys(p.R1155C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48816233:48816233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1586G>T
AA Mutation	p.Arg529Leu(p.R529L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48816164:48816164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1517G>A
AA Mutation	p.Arg506His(p.R506H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48820151:48820151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782734600
CDS Mutation	c.2233C>T
AA Mutation	p.Arg745Trp(p.R745W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48822785:48822785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782041149
CDS Mutation	c.2503C>T
AA Mutation	p.Arg835Trp(p.R835W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48820191:48820191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2273G>T
AA Mutation	p.Gly758Val(p.G758V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48814684:48814684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943C>T
AA Mutation	p.Arg315Trp(p.R315W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48823439:48823439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3040G>A
AA Mutation	p.Gly1014Arg(p.G1014R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48806684:48806684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610C>T
AA Mutation	p.Arg204Trp(p.R204W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48817425:48817425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1891C>T
AA Mutation	p.Arg631Cys(p.R631C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334136
Start	48814887:48814887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334136
Start	48816231:48816231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781831075
CDS Mutation	c.1584G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334136
Start	48815933:48815933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150105386
CDS Mutation	c.1374C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334136
Start	48820192:48820192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2274T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334136
Start	48820165:48820165(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2252delG
AA Mutation	p.Gly751AlafsTer16(p.G751Afs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HDAC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48823350:48823350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2951C>T
AA Mutation	p.Ala984Val(p.A984V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48802911:48802911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134C>A
AA Mutation	p.Pro45His(p.P45H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334136
Start	48823528:48823528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781903016
CDS Mutation	c.3129G>T
AA Mutation	p.Gln1043His(p.Q1043H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334136
Start	48816570:48816570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1728C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334136
Start	48814524:48814524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782212703
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334136
Start	48818301:48818301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2076C>A
Mutation Classification	Silent
Feature Type	Transcript