Colon Cancer: Gene >> KLB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39434313:39434313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201377023
CDS Mutation	c.929C>T
AA Mutation	p.Ser310Leu(p.S310L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39407686:39407686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.737C>T
AA Mutation	p.Ala246Val(p.A246V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39446446:39446446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1720G>A
AA Mutation	p.Ala574Thr(p.A574T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39448471:39448471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2920T>C
AA Mutation	p.Ser974Pro(p.S974P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39434385:39434385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001T>G
AA Mutation	p.Ile334Ser(p.I334S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39434491:39434491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767539660
CDS Mutation	c.1107C>A
AA Mutation	p.Phe369Leu(p.F369L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39446852:39446852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2126A>G
AA Mutation	p.Tyr709Cys(p.Y709C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39446345:39446345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1619C>T
AA Mutation	p.Ala540Val(p.A540V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39437978:39437978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1588A>G
AA Mutation	p.Thr530Ala(p.T530A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39448369:39448369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2818C>T
AA Mutation	p.Pro940Ser(p.P940S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257408
Start	39447174:39447174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2448C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257408
Start	39447300:39447300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2574C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257408
Start	39446727:39446727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2001C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257408
Start	39446634:39446634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267600149
CDS Mutation	c.1908C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257408
Start	39448557:39448557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3006T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257408
Start	39446601:39446601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1875C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257408
Start	39437959:39437959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1569T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257408
Start	39446556:39446556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775336960
CDS Mutation	c.1830C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KLB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39448468:39448468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2917A>G
AA Mutation	p.Ser973Gly(p.S973G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39407736:39407736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.787T>G
AA Mutation	p.Leu263Val(p.L263V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257408
Start	39407098:39407098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.149T>G
AA Mutation	p.Val50Gly(p.V50G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257408
Start	39446520:39446520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1794G>C
Mutation Classification	Silent
Feature Type	Transcript