Colon Cancer: Gene >> ZNF135

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58066863:58066863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379G>A
AA Mutation	p.Glu127Lys(p.E127K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58066945:58066945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746765542
CDS Mutation	c.461C>T
AA Mutation	p.Thr154Met(p.T154M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58067464:58067464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.980A>C
AA Mutation	p.Glu327Ala(p.E327A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58066920:58066920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.436C>T
AA Mutation	p.Pro146Ser(p.P146S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58067625:58067625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184985935
CDS Mutation	c.1141C>T
AA Mutation	p.Pro381Ser(p.P381S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58061589:58061589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43A>G
AA Mutation	p.Thr15Ala(p.T15A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58061590:58061590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44C>T
AA Mutation	p.Thr15Met(p.T15M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58067490:58067490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117003717
CDS Mutation	c.1006C>T
AA Mutation	p.Arg336Trp(p.R336W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58067169:58067169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685C>A
AA Mutation	p.Leu229Ile(p.L229I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58068339:58068339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1855A>G
AA Mutation	p.Thr619Ala(p.T619A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58066884:58066884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400G>A
AA Mutation	p.Glu134Lys(p.E134K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58067388:58067388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536588023
CDS Mutation	c.904G>A
AA Mutation	p.Glu302Lys(p.E302K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000313434
Start	58068312:58068312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140244919
CDS Mutation	c.1828G>A
AA Mutation	p.Asp610Asn(p.D610N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313434
Start	58068308:58068308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1824T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313434
Start	58067129:58067129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs8106659
CDS Mutation	c.645A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313434
Start	58068281:58068281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749552931
CDS Mutation	c.1797G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313434
Start	58068272:58068272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2228276
CDS Mutation	c.1788C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313434
Start	58067594:58067594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000313434
Start	58067985:58067985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1501A>T
AA Mutation	p.Lys501Ter(p.K501*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF135

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313434
Start	58063459:58063459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375491279
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313434
Start	58067888:58067888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766152094
CDS Mutation	c.1404C>T
Mutation Classification	Silent
Feature Type	Transcript