Colon Cancer: Gene >> HNRNPDL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295470
Start	82426622:82426622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033A>T
AA Mutation	p.Asn345Tyr(p.N345Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295470
Start	82426067:82426067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1255C>A
AA Mutation	p.Pro419Thr(p.P419T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295470
Start	82428143:82428143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649T>G
AA Mutation	p.Leu217Val(p.L217V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295470
Start	82429259:82429259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432G>T
AA Mutation	p.Gln144His(p.Q144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295470
Start	82429311:82429311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752922266
CDS Mutation	c.380G>A
AA Mutation	p.Ser127Asn(p.S127N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295470
Start	82429280:82429280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.411G>T
AA Mutation	p.Lys137Asn(p.K137N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295470
Start	82429354:82429354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141595181
CDS Mutation	c.337C>T
AA Mutation	p.Pro113Ser(p.P113S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295470
Start	82428033:82428033(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.759delT
AA Mutation	p.Phe253LeufsTer35(p.F253Lfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295470
Start	82427472:82427472(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.867delA
AA Mutation	p.Lys289AsnfsTer3(p.K289Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295470
Start	82426093:82426093(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1229delG
AA Mutation	p.Gly410ValfsTer25(p.G410Vfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000295470
Start	82426100:82426100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1222C>T
AA Mutation	p.Arg408Ter(p.R408*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000295470
Start	82427486:82427486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.853G>T
AA Mutation	p.Glu285Ter(p.E285*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295470
Start	82427471:82427472(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.867dupA
AA Mutation	p.Leu290IlefsTer15(p.L290Ifs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPDL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295470
Start	82429410:82429410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281C>G
AA Mutation	p.Ser94Cys(p.S94C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295470
Start	82428331:82428331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559A>C
Mutation Classification	Silent
Feature Type	Transcript