Colon Cancer: Gene >> HIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336926
Start	75545156:75545156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2592G>T
AA Mutation	p.Lys864Asn(p.K864N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336926
Start	75559837:75559837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1270C>A
AA Mutation	p.Gln424Lys(p.Q424K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336926
Start	75592069:75592069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.371T>C
AA Mutation	p.Met124Thr(p.M124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336926
Start	75592401:75592401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298C>T
AA Mutation	p.His100Tyr(p.H100Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336926
Start	75562110:75562110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1081A>G
AA Mutation	p.Asn361Asp(p.N361D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336926
Start	75559781:75559781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1326G>T
AA Mutation	p.Arg442Ser(p.R442S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336926
Start	75557688:75557688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547C>T
AA Mutation	p.Ser516Leu(p.S516L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336926
Start	75559887:75559887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1220G>A
AA Mutation	p.Gly407Asp(p.G407D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336926
Start	75556157:75556157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1696T>C
AA Mutation	p.Trp566Arg(p.W566R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000336926
Start	75541951:75541951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2920A>T
AA Mutation	p.Thr974Ser(p.T974S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336926
Start	75553456:75553456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782381013
CDS Mutation	c.2292C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336926
Start	75556143:75556143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1710C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336926
Start	75562983:75562983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336926
Start	75559766:75559766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1341C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336926
Start	75556029:75556029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1824A>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336926
Start	75573862:75573862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368324123
CDS Mutation	c.644C>T
AA Mutation	p.Thr215Met(p.T215M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336926
Start	75562085:75562085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1106A>G
AA Mutation	p.Asn369Ser(p.N369S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336926
Start	75556095:75556095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143541649
CDS Mutation	c.1758T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000336926
Start	75539413:75539413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2971G>T
AA Mutation	p.Glu991Ter(p.E991*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000336926
Start	75582094:75582094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523G>T
AA Mutation	p.Glu175Ter(p.E175*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript