Colon Cancer: Gene >> HIRA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19383663:19383663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1372C>T
AA Mutation	p.Arg458Trp(p.R458W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19357022:19357022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2264G>A
AA Mutation	p.Arg755Lys(p.R755K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19385711:19385711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1139G>A
AA Mutation	p.Gly380Asp(p.G380D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19392202:19392202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.835A>C
AA Mutation	p.Lys279Gln(p.K279Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19407257:19407257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229C>T
AA Mutation	p.Arg77Trp(p.R77W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19375662:19375662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744C>A
AA Mutation	p.Leu582Met(p.L582M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19394485:19394485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.679C>T
AA Mutation	p.Arg227Trp(p.R227W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19378031:19378031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1451T>C
AA Mutation	p.Leu484Pro(p.L484P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19405824:19405824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359A>G
AA Mutation	p.Gln120Arg(p.Q120R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19385667:19385667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745364733
CDS Mutation	c.1183G>A
AA Mutation	p.Val395Ile(p.V395I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19394379:19394379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.785T>C
AA Mutation	p.Met262Thr(p.M262T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19405876:19405876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307A>G
AA Mutation	p.Ile103Val(p.I103V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19398054:19398054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431C>T
AA Mutation	p.Ala144Val(p.A144V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19354057:19354057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2623C>T
AA Mutation	p.Pro875Ser(p.P875S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19405841:19405841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.342G>T
AA Mutation	p.Lys114Asn(p.K114N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19361251:19361251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2071G>A
AA Mutation	p.Ala691Thr(p.A691T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19359345:19359345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774636516
CDS Mutation	c.2225C>T
AA Mutation	p.Ala742Val(p.A742V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263208
Start	19388537:19388537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.954G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263208
Start	19410732:19410732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263208
Start	19361894:19361894(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1813delC
AA Mutation	p.Arg605GlufsTer31(p.R605Efs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000263208
Start	19385634:19385634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1216C>T
AA Mutation	p.Arg406Ter(p.R406*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000263208
Start	19351429:19351429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2866C>T
AA Mutation	p.Arg956Ter(p.R956*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000263208
Start	19385612:19385613(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs746667249
CDS Mutation	c.1235_1237dupAGC
AA Mutation	p.Gln412dup(p.Q412dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HIRA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19375715:19375715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1691C>T
AA Mutation	p.Ala564Val(p.A564V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19375692:19375692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1714C>T
AA Mutation	p.Arg572Trp(p.R572W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263208
Start	19353365:19353365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782473677
CDS Mutation	c.2839G>A
AA Mutation	p.Val947Ile(p.V947I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263208
Start	19377946:19377946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759228734
CDS Mutation	c.1536C>T
Mutation Classification	Silent
Feature Type	Transcript