Colon Cancer: Gene >> ZC3HC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130023662:130023662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082T>C
AA Mutation	p.Val361Ala(p.V361A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130040990:130040990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.370C>T
AA Mutation	p.Leu124Phe(p.L124F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130026164:130026164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764600804
CDS Mutation	c.770C>T
AA Mutation	p.Ala257Val(p.A257V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130028970:130028970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143076145
CDS Mutation	c.553C>T
AA Mutation	p.Arg185Cys(p.R185C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130026249:130026249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685A>T
AA Mutation	p.Thr229Ser(p.T229S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130029000:130029000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523C>G
AA Mutation	p.Pro175Ala(p.P175A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130028928:130028928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.595C>A
AA Mutation	p.Leu199Ile(p.L199I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130024349:130024349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934C>T
AA Mutation	p.Pro312Ser(p.P312S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130049064:130049064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227A>T
AA Mutation	p.Glu76Val(p.E76V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130039544:130039544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413A>T
AA Mutation	p.Lys138Met(p.K138M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358303
Start	130024392:130024392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358303
Start	130024470:130024470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358303
Start	130022406:130022406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767502846
CDS Mutation	c.1353C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZC3HC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130022505:130022505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254C>A
AA Mutation	p.Phe418Leu(p.F418L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130023602:130023602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142G>C
AA Mutation	p.Ser381Thr(p.S381T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130018693:130018693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777832847
CDS Mutation	c.1480C>T
AA Mutation	p.Arg494Trp(p.R494W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130028966:130028966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557T>G
AA Mutation	p.Phe186Cys(p.F186C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358303
Start	130051342:130051342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25G>T
AA Mutation	p.Ala9Ser(p.A9S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358303
Start	130049114:130049114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177T>G
Mutation Classification	Silent
Feature Type	Transcript