Colon Cancer: Gene >> ASIC1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000447966
Start	50078002:50078002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759280738
CDS Mutation	c.712G>A
AA Mutation	p.Glu238Lys(p.E238K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000447966
Start	50078081:50078081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791G>A
AA Mutation	p.Gly264Asp(p.G264D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000447966
Start	50077265:50077265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767028389
CDS Mutation	c.611G>A
AA Mutation	p.Arg204Gln(p.R204Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000447966
Start	50078530:50078530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200645931
CDS Mutation	c.947C>T
AA Mutation	p.Thr316Met(p.T316M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000447966
Start	50059115:50059115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>A
AA Mutation	p.Leu117Met(p.L117M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000447966
Start	50081627:50081627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1565C>T
AA Mutation	p.Thr522Met(p.T522M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000447966
Start	50078927:50078927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998A>G
AA Mutation	p.Asp333Gly(p.D333G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000447966
Start	50059038:50059038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.272C>T
AA Mutation	p.Thr91Met(p.T91M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447966
Start	50078115:50078115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447966
Start	50077335:50077335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201565651
CDS Mutation	c.681C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447966
Start	50078082:50078082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149923094
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447966
Start	50078937:50078937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750767632
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ASIC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000447966
Start	50078965:50078965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1036G>A
AA Mutation	p.Ala346Thr(p.A346T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447966
Start	50078013:50078013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775463015
CDS Mutation	c.723C>T
Mutation Classification	Silent
Feature Type	Transcript