Colon Cancer: Gene >> DMPK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000291270
Start	45779515:45779515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260T>C
AA Mutation	p.Val87Ala(p.V87A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000291270
Start	45778544:45778544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530C>T
AA Mutation	p.Ala177Val(p.A177V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000291270
Start	45770610:45770610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1768T>C
AA Mutation	p.Ser590Pro(p.S590P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000291270
Start	45778559:45778559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199731275
CDS Mutation	c.515C>T
AA Mutation	p.Ala172Val(p.A172V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000291270
Start	45777541:45777541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201714957
CDS Mutation	c.932G>A
AA Mutation	p.Arg311Gln(p.R311Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000291270
Start	45778592:45778592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482G>T
AA Mutation	p.Ser161Ile(p.S161I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000291270
Start	45777747:45777747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376004763
CDS Mutation	c.802G>A
AA Mutation	p.Ala268Thr(p.A268T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291270
Start	45779814:45779814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291270
Start	45778160:45778160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367743734
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291270
Start	45777399:45777399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369938946
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291270
Start	45777564:45777564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200058479
CDS Mutation	c.909C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291270
Start	45778558:45778558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748808453
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291270
Start	45778510:45778510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DMPK

No Mutation Annotation!