Colon Cancer: Gene >> CLDN10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299339
Start	95552847:95552847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94G>T
AA Mutation	p.Val32Leu(p.V32L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376873
Start	95433873:95433873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40G>A
AA Mutation	p.Gly14Arg(p.G14R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376873
Start	95433964:95433964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.131A>G
AA Mutation	p.Tyr44Cys(p.Y44C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299339
Start	95552863:95552863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.110G>A
AA Mutation	p.Gly37Asp(p.G37D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299339
Start	95577917:95577917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590C>T
AA Mutation	p.Ala197Val(p.A197V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376873
Start	95433943:95433943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110T>C
AA Mutation	p.Val37Ala(p.V37A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000299339
Start	95560437:95560437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438C>A
AA Mutation	p.Phe146Leu(p.F146L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376873
Start	95433986:95433986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000299339
Start	95552975:95552975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.220+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CLDN10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299339
Start	95560437:95560437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438C>A
AA Mutation	p.Phe146Leu(p.F146L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript