Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZNF24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261332
Start	35337291:35337291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048C>A
AA Mutation	p.Leu350Ile(p.L350I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261332
Start	35337359:35337359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980G>T
AA Mutation	p.Arg327Ile(p.R327I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261332
Start	35340463:35340463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188C>T
AA Mutation	p.Ser63Leu(p.S63L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261332
Start	35340557:35340557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.94C>G
AA Mutation	p.Pro32Ala(p.P32A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261332
Start	35339963:35339963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781423777
CDS Mutation	c.434G>A
AA Mutation	p.Arg145Gln(p.R145Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261332
Start	35340297:35340297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.354G>T
AA Mutation	p.Glu118Asp(p.E118D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261332
Start	35337498:35337498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841T>C
AA Mutation	p.Cys281Arg(p.C281R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_lost
Transcription ID	ENST00000261332
Start	35337233:35337233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1106A>T
AA Mutation	p.Ter369LeuextTer22(p.369Lext22)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261332
Start	35337527:35337527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812G>T
AA Mutation	p.Arg271Ile(p.R271I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261332
Start	35337380:35337380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.959C>T
AA Mutation	p.Ser320Leu(p.S320L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261332
Start	35339937:35339937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460G>T
AA Mutation	p.Asp154Tyr(p.D154Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261332
Start	35337359:35337359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980G>T
AA Mutation	p.Arg327Ile(p.R327I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript