Colon Cancer: Gene >> HAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264108
Start	171966884:171966884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758G>A
AA Mutation	p.Gly253Asp(p.G253D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264108
Start	171983264:171983264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172T>C
AA Mutation	p.Ile391Thr(p.I391T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264108
Start	171976238:171976238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760798004
CDS Mutation	c.905G>A
AA Mutation	p.Arg302Gln(p.R302Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264108
Start	171965866:171965866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569G>C
AA Mutation	p.Ser190Thr(p.S190T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264108
Start	171925635:171925635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106A>C
AA Mutation	p.Lys36Gln(p.K36Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264108
Start	171965435:171965435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.407T>C
AA Mutation	p.Phe136Ser(p.F136S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264108
Start	171952941:171952941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.249G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264108
Start	171946738:171946739(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.143_144insATTCC
AA Mutation	p.Arg49PhefsTer26(p.R49Ffs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000264108
Start	171946707:171946707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.113-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> HAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264108
Start	171925553:171925553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.24G>T
AA Mutation	p.Glu8Asp(p.E8D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264108
Start	171965445:171965445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533334266
CDS Mutation	c.417C>T
Mutation Classification	Silent
Feature Type	Transcript