Colon Cancer: Gene >> ATP6AP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369762
Start	154435290:154435290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375162515
CDS Mutation	c.988C>T
AA Mutation	p.Arg330Cys(p.R330C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369762
Start	154434248:154434248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.725G>A
AA Mutation	p.Arg242His(p.R242H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369762
Start	154432395:154432395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782026906
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Trp(p.R165W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369762
Start	154429070:154429070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.184G>A
AA Mutation	p.Asp62Asn(p.D62N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369762
Start	154432374:154432374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.472C>T
AA Mutation	p.His158Tyr(p.H158Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369762
Start	154434353:154434353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830C>T
AA Mutation	p.Ala277Val(p.A277V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369762
Start	154428731:154428731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375325990
CDS Mutation	c.39G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369762
Start	154434339:154434339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.816A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ATP6AP1

No Mutation Annotation!