Colon Cancer: Gene >> GHR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42699929:42699929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545A>C
AA Mutation	p.Asp182Ala(p.D182A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42718116:42718116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940C>A
AA Mutation	p.Leu314Ile(p.L314I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42718774:42718774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1267C>A
AA Mutation	p.Leu423Ile(p.L423I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42719381:42719381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1874G>A
AA Mutation	p.Cys625Tyr(p.C625Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42695075:42695075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.425C>T
AA Mutation	p.Ser142Phe(p.S142F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42699857:42699857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473C>A
AA Mutation	p.Thr158Asn(p.T158N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42718963:42718963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1456T>G
AA Mutation	p.Phe486Val(p.F486V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42688984:42688984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231G>T
AA Mutation	p.Lys77Asn(p.K77N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42694937:42694937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287A>G
AA Mutation	p.Gln96Arg(p.Q96R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42688923:42688923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373412197
CDS Mutation	c.170G>A
AA Mutation	p.Arg57His(p.R57H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42719339:42719339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775194712
CDS Mutation	c.1832C>T
AA Mutation	p.Ala611Val(p.A611V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230882
Start	42719295:42719295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1788C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230882
Start	42711311:42711311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230882
Start	42688921:42688921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GHR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42718634:42718634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1127A>G
AA Mutation	p.Asn376Ser(p.N376S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42719072:42719072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1565C>T
AA Mutation	p.Ser522Leu(p.S522L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000230882
Start	42711358:42711358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.770T>G
AA Mutation	p.Phe257Cys(p.F257C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230882
Start	42719070:42719070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230882
Start	42695022:42695022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372T>G
Mutation Classification	Silent
Feature Type	Transcript