Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BRDT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91991226:91991226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2045C>T
AA Mutation	p.Pro682Leu(p.P682L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	92014236:92014236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2806A>G
AA Mutation	p.Ser936Gly(p.S936G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91964681:91964681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.247T>G
AA Mutation	p.Leu83Val(p.L83V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91977358:91977358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934G>A
AA Mutation	p.Val312Ile(p.V312I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91979595:91979595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125G>T
AA Mutation	p.Lys375Asn(p.K375N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91980732:91980732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1377G>T
AA Mutation	p.Lys459Asn(p.K459N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91992301:91992301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2102C>G
AA Mutation	p.Thr701Arg(p.T701R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91976328:91976328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508A>C
AA Mutation	p.Lys170Gln(p.K170Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91980927:91980927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1499A>C
AA Mutation	p.Lys500Thr(p.K500T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	92005249:92005249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2725G>T
AA Mutation	p.Asp909Tyr(p.D909Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362005
Start	91991227:91991227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2046T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362005
Start	91979577:91979577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000362005
Start	91976346:91976346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.526G>T
AA Mutation	p.Glu176Ter(p.E176*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> BRDT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91977358:91977358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934G>A
AA Mutation	p.Val312Ile(p.V312I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	92005159:92005159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2635A>G
AA Mutation	p.Lys879Glu(p.K879E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91964678:91964678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244C>T
AA Mutation	p.Arg82Cys(p.R82C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91964646:91964646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765131878
CDS Mutation	c.212A>C
AA Mutation	p.Lys71Thr(p.K71T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91977162:91977162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738A>C
AA Mutation	p.Lys246Asn(p.K246N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000362005
Start	91980722:91980722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1367A>C
AA Mutation	p.Lys456Thr(p.K456T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362005
Start	91977282:91977282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000362005
Start	91979577:91979577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000362005
Start	91968221:91968221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.406G>T
AA Mutation	p.Glu136Ter(p.E136*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript