Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ATG4C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317868
Start	62819196:62819196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586T>G
AA Mutation	p.Tyr196Asp(p.Y196D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317868
Start	62821167:62821167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754G>T
AA Mutation	p.Asp252Tyr(p.D252Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317868
Start	62841504:62841504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759584462
CDS Mutation	c.1166G>A
AA Mutation	p.Arg389Gln(p.R389Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317868
Start	62819276:62819276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666G>T
AA Mutation	p.Lys222Asn(p.K222N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317868
Start	62803858:62803858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72A>C
AA Mutation	p.Lys24Asn(p.K24N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317868
Start	62834810:62834810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763822053
CDS Mutation	c.1047C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317868
Start	62816636:62816636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000317868
Start	62819118:62819118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508G>T
AA Mutation	p.Glu170Ter(p.E170*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ATG4C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317868
Start	62819036:62819036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747792609
CDS Mutation	c.426A>C
AA Mutation	p.Glu142Asp(p.E142D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317868
Start	62841504:62841504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759584462
CDS Mutation	c.1166G>A
AA Mutation	p.Arg389Gln(p.R389Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317868
Start	62864094:62864095(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1318dupT
AA Mutation	p.Ser440PhefsTer4(p.S440Ffs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript