Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ARNTL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266503
Start	27401577:27401577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321G>T
AA Mutation	p.Asp441Tyr(p.D441Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266503
Start	27380273:27380273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353G>A
AA Mutation	p.Arg118Gln(p.R118Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266503
Start	27368379:27368379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780181750
CDS Mutation	c.149G>A
AA Mutation	p.Arg50Gln(p.R50Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266503
Start	27418143:27418143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11049005
CDS Mutation	c.1721C>T
AA Mutation	p.Ala574Val(p.A574V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266503
Start	27403439:27403439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1484C>T
AA Mutation	p.Ser495Phe(p.S495F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266503
Start	27420405:27420405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1784C>T
AA Mutation	p.Ala595Val(p.A595V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266503
Start	27390213:27390213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.893G>T
AA Mutation	p.Gly298Val(p.G298V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000266503
Start	27401360:27401360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1264G>A
AA Mutation	p.Ala422Thr(p.A422T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000266503
Start	27400650:27400650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1036C>A
AA Mutation	p.Leu346Ile(p.L346I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000266503
Start	27368313:27368313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756988598
CDS Mutation	c.83G>A
AA Mutation	p.Arg28His(p.R28H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266503
Start	27380343:27380343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369489279
CDS Mutation	c.423G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266503
Start	27402622:27402622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1422A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266503
Start	27387281:27387281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758363984
CDS Mutation	c.618C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266503
Start	27390220:27390220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000266503
Start	27401609:27401609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353G>A
AA Mutation	p.Trp451Ter(p.W451*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266503
Start	27390162:27390163(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.848dupT
AA Mutation	p.Cys284LeufsTer7(p.C284Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000266503
Start	27415868:27415869(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1587_1596dupGTTACAGTCT
AA Mutation	p.Ser533ValfsTer8(p.S533Vfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000266503
Start	27415868:27415868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1587-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	inframe_insertion;splice_region_variant
Transcription ID	ENST00000266503
Start	27376345:27376346(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.288_308dupGGAAGATGGTGAACACCAAGT
AA Mutation	p.Glu97_Val103dup(p.E97_V103dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_lost
Transcription ID	ENST00000266503
Start	27420531:27420531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1910A>G
AA Mutation	p.Ter637TrpextTer37(p.637Wext37)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ARNTL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266503
Start	27380269:27380269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349A>G
AA Mutation	p.Lys117Glu(p.K117E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266503
Start	27385493:27385493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.497C>A
AA Mutation	p.Ser166Tyr(p.S166Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266503
Start	27390193:27390193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.873C>A
Mutation Classification	Silent
Feature Type	Transcript