Colon Cancer: Gene >> HRG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186677117:186677117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812C>A
AA Mutation	p.Ser271Tyr(p.S271Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186668987:186668987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs4516605
CDS Mutation	c.236C>T
AA Mutation	p.Ser79Leu(p.S79L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186677736:186677736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1431T>G
AA Mutation	p.Phe477Leu(p.F477L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186677368:186677368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1063C>A
AA Mutation	p.His355Asn(p.H355N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186677701:186677701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1396A>C
AA Mutation	p.Lys466Gln(p.K466Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186677755:186677755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1450C>T
AA Mutation	p.His484Tyr(p.H484Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186677812:186677812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1507T>A
AA Mutation	p.Ser503Thr(p.S503T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186675182:186675182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201213205
CDS Mutation	c.733G>A
AA Mutation	p.Asp245Asn(p.D245N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186666117:186666117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756432163
CDS Mutation	c.86C>T
AA Mutation	p.Pro29Leu(p.P29L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186677455:186677455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1150C>T
AA Mutation	p.His384Tyr(p.H384Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186671672:186671672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764549526
CDS Mutation	c.441C>A
AA Mutation	p.Phe147Leu(p.F147L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186675147:186675147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.698G>T
AA Mutation	p.Ser233Ile(p.S233I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186677674:186677674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1369T>A
AA Mutation	p.Ser457Thr(p.S457T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186669037:186669037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539629653
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Cys(p.R96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232003
Start	186677289:186677289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754842733
CDS Mutation	c.984A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232003
Start	186677235:186677235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232003
Start	186677073:186677073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193295280
CDS Mutation	c.768G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232003
Start	186675151:186675151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201536659
CDS Mutation	c.702G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232003
Start	186672813:186672813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193063661
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000232003
Start	186671766:186671766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145379172
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Ter(p.R179*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HRG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186666084:186666084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.53C>A
AA Mutation	p.Ala18Asp(p.A18D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186677212:186677212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759137427
CDS Mutation	c.907G>A
AA Mutation	p.Glu303Lys(p.E303K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186677296:186677296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.991A>C
AA Mutation	p.Thr331Pro(p.T331P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000232003
Start	186677216:186677216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.911G>T
AA Mutation	p.Arg304Ile(p.R304I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000232003
Start	186677626:186677626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370685538
CDS Mutation	c.1321C>T
AA Mutation	p.Arg441Ter(p.R441*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript