Colon Cancer: Gene >> ZNF350

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243644
Start	51965852:51965852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601A>C
AA Mutation	p.Lys201Gln(p.K201Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243644
Start	51968655:51968655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199891932
CDS Mutation	c.161C>T
AA Mutation	p.Pro54Leu(p.P54L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000243644
Start	51965386:51965386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067C>A
AA Mutation	p.Ser356Tyr(p.S356Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000243644
Start	51965722:51965722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.731C>T
AA Mutation	p.Ser244Phe(p.S244F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000243644
Start	51964895:51964895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148220969
CDS Mutation	c.1558G>A
AA Mutation	p.Val520Met(p.V520M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000243644
Start	51965100:51965100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353G>A
AA Mutation	p.Met451Ile(p.M451I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000243644
Start	51965524:51965524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781302955
CDS Mutation	c.929G>A
AA Mutation	p.Arg310Gln(p.R310Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000243644
Start	51969055:51969055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.92A>G
AA Mutation	p.Asp31Gly(p.D31G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000243644
Start	51965024:51965024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759224562
CDS Mutation	c.1429G>A
AA Mutation	p.Gly477Ser(p.G477S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243644
Start	51965625:51965625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.828G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243644
Start	51965079:51965079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542665274
CDS Mutation	c.1374C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000243644
Start	51965342:51965342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111G>T
AA Mutation	p.Glu371Ter(p.E371*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF350

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243644
Start	51965356:51965356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566120255
CDS Mutation	c.1097G>T
AA Mutation	p.Arg366Ile(p.R366I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243644
Start	51965797:51965797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.656C>A
AA Mutation	p.Ser219Tyr(p.S219Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000243644
Start	51965941:51965941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138780746
CDS Mutation	c.512G>A
AA Mutation	p.Arg171Gln(p.R171Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript