Colon Cancer: Gene >> STK17A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319357
Start	43623834:43623834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.866T>C
AA Mutation	p.Val289Ala(p.V289A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319357
Start	43608339:43608339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77026432
CDS Mutation	c.503G>A
AA Mutation	p.Arg168Gln(p.R168Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319357
Start	43583251:43583251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>T
AA Mutation	p.Pro3Leu(p.P3L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319357
Start	43624658:43624658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061C>T
AA Mutation	p.Ser354Leu(p.S354L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319357
Start	43624771:43624771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174A>C
AA Mutation	p.Lys392Gln(p.K392Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000319357
Start	43595975:43595975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281A>G
AA Mutation	p.Lys94Arg(p.K94R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319357
Start	43623733:43623733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.765C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319357
Start	43624734:43624734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1137A>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> STK17A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319357
Start	43623859:43623859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891C>A
AA Mutation	p.Phe297Leu(p.F297L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript