Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DMRTB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371445
Start	53461499:53461499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767242421
CDS Mutation	c.604C>T
AA Mutation	p.Arg202Cys(p.R202C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371445
Start	53464686:53464686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.800C>T
AA Mutation	p.Pro267Leu(p.P267L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371445
Start	53461476:53461476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370607830
CDS Mutation	c.581G>A
AA Mutation	p.Arg194His(p.R194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371445
Start	53459585:53459585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.132C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371445
Start	53459636:53459636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201603810
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371445
Start	53464783:53464783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761203609
CDS Mutation	c.897G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371445
Start	53464771:53464771(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.890delC
AA Mutation	p.Pro297ArgfsTer13(p.P297Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DMRTB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371445
Start	53461476:53461476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370607830
CDS Mutation	c.581G>A
AA Mutation	p.Arg194His(p.R194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371445
Start	53464807:53464807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.921C>A
AA Mutation	p.Phe307Leu(p.F307L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371445
Start	53461573:53461573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769317497
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000371445
Start	53466619:53466619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.986C>A
AA Mutation	p.Ser329Ter(p.S329*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript