Colon Cancer: Gene >> PUF60

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000526683
Start	143817118:143817118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172C>T
AA Mutation	p.Pro391Leu(p.P391L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000526683
Start	143824339:143824339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85G>A
AA Mutation	p.Ala29Thr(p.A29T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000526683
Start	143818390:143818390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756023794
CDS Mutation	c.493G>A
AA Mutation	p.Val165Ile(p.V165I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000526683
Start	143817381:143817381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094G>A
AA Mutation	p.Gly365Asp(p.G365D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000526683
Start	143817454:143817454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1021G>A
AA Mutation	p.Gly341Arg(p.G341R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000526683
Start	143817128:143817128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162C>T
AA Mutation	p.Pro388Ser(p.P388S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000526683
Start	143816731:143816731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1469T>C
AA Mutation	p.Phe490Ser(p.F490S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000526683
Start	143817991:143817991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688G>A
AA Mutation	p.Val230Met(p.V230M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526683
Start	143817114:143817114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1176C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526683
Start	143816937:143816937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526683
Start	143817446:143817446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368804058
CDS Mutation	c.1029G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000526683
Start	143818206:143818206(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.590delG
AA Mutation	p.Gly197AlafsTer12(p.G197Afs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000526683
Start	143818483:143818512(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.371_400delCGCTGGCCATCATGTGCCGCGTCTACGTGG
AA Mutation	p.Ala124_Val133del(p.A124_V133del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PUF60

No Mutation Annotation!