Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DZIP1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138094971:138094971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599A>T
AA Mutation	p.Lys200Ile(p.K200I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138103613:138103613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777975721
CDS Mutation	c.359G>A
AA Mutation	p.Gly120Asp(p.G120D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138062870:138062870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2250G>T
AA Mutation	p.Glu750Asp(p.E750D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138092468:138092468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.785A>C
AA Mutation	p.Lys262Thr(p.K262T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138103520:138103520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452G>T
AA Mutation	p.Ser151Ile(p.S151I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138071733:138071733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1525A>G
AA Mutation	p.Arg509Gly(p.R509G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138080602:138080602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1253A>T
AA Mutation	p.Lys418Met(p.K418M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138067605:138067605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754376571
CDS Mutation	c.1928G>A
AA Mutation	p.Arg643Gln(p.R643Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138103922:138103922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50G>A
AA Mutation	p.Gly17Glu(p.G17E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138068333:138068333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1650G>T
AA Mutation	p.Glu550Asp(p.E550D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138103658:138103658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314G>A
AA Mutation	p.Ser105Asn(p.S105N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138094967:138094967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603G>T
AA Mutation	p.Gln201His(p.Q201H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138103863:138103863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139394665
CDS Mutation	c.109C>T
AA Mutation	p.Arg37Cys(p.R37C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138094973:138094973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.597G>T
AA Mutation	p.Lys199Asn(p.K199N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327532
Start	138064634:138064634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2136G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327532
Start	138068219:138068219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141369259
CDS Mutation	c.1764C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327532
Start	138103684:138103684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327532
Start	138092413:138092413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.840T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327532
Start	138067606:138067606(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1927delC
AA Mutation	p.Arg643GlyfsTer40(p.R643Gfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327532
Start	138092436:138092437(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.816dupA
AA Mutation	p.Leu273IlefsTer5(p.L273Ifs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DZIP1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138092439:138092439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.814A>C
AA Mutation	p.Lys272Gln(p.K272Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138086967:138086967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1056G>T
AA Mutation	p.Lys352Asn(p.K352N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327532
Start	138077597:138077597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1324C>T
Mutation Classification	Silent
Feature Type	Transcript