Colon Cancer: Gene >> NKD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296849
Start	1033375:1033375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206C>T
AA Mutation	p.Ala69Val(p.A69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296849
Start	1038239:1038239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1222C>T
AA Mutation	p.His408Tyr(p.H408Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296849
Start	1033446:1033446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.277G>A
AA Mutation	p.Ala93Thr(p.A93T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296849
Start	1037978:1037978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961C>T
AA Mutation	p.Pro321Ser(p.P321S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296849
Start	1037961:1037961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375289481
CDS Mutation	c.944G>A
AA Mutation	p.Arg315Gln(p.R315Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296849
Start	1034852:1034852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199906392
CDS Mutation	c.523G>A
AA Mutation	p.Val175Ile(p.V175I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296849
Start	1038199:1038199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296849
Start	1033475:1033475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76765500
CDS Mutation	c.306G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NKD2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296849
Start	1038370:1038370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353C>G
Mutation Classification	Silent
Feature Type	Transcript