Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DPY19L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310974
Start	34957991:34957991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.953T>G
AA Mutation	p.Ile318Ser(p.I318S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310974
Start	34958044:34958044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900G>C
AA Mutation	p.Leu300Phe(p.L300F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310974
Start	35017950:35017950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124T>A
AA Mutation	p.Phe42Ile(p.F42I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310974
Start	34954714:34954714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1085T>G
AA Mutation	p.Phe362Cys(p.F362C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310974
Start	34949866:34949866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134C>A
AA Mutation	p.Phe378Leu(p.F378L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310974
Start	34954763:34954763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1036T>C
AA Mutation	p.Phe346Leu(p.F346L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310974
Start	35013575:35013575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323A>G
AA Mutation	p.Tyr108Cys(p.Y108C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310974
Start	35017966:35017966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DPY19L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310974
Start	34954765:34954765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1034G>A
AA Mutation	p.Cys345Tyr(p.C345Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310974
Start	34966916:34966916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774134203
CDS Mutation	c.851G>A
AA Mutation	p.Arg284Gln(p.R284Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310974
Start	34945681:34945681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1311A>T
AA Mutation	p.Gln437His(p.Q437H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310974
Start	34949866:34949866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134C>A
AA Mutation	p.Phe378Leu(p.F378L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310974
Start	35017892:35017892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.182G>A
AA Mutation	p.Arg61His(p.R61H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript