Colon Cancer: Gene >> VPS4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254950
Start	69320754:69320754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769562853
CDS Mutation	c.836C>T
AA Mutation	p.Ser279Leu(p.S279L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254950
Start	69316245:69316245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.154G>A
AA Mutation	p.Ala52Thr(p.A52T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254950
Start	69319405:69319405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536870010
CDS Mutation	c.482G>A
AA Mutation	p.Arg161Gln(p.R161Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254950
Start	69320244:69320244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724G>A
AA Mutation	p.Glu242Lys(p.E242K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254950
Start	69322662:69322662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780605736
CDS Mutation	c.1174G>A
AA Mutation	p.Val392Ile(p.V392I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254950
Start	69324260:69324260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1265A>G
AA Mutation	p.Asp422Gly(p.D422G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000254950
Start	69321095:69321095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771707990
CDS Mutation	c.896G>A
AA Mutation	p.Arg299His(p.R299H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000254950
Start	69320199:69320199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.679G>A
AA Mutation	p.Asp227Asn(p.D227N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000254950
Start	69320152:69320152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632A>G
AA Mutation	p.Asn211Ser(p.N211S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> VPS4A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254950
Start	69320273:69320273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753C>A
AA Mutation	p.Phe251Leu(p.F251L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254950
Start	69316238:69316238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746250461
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript