Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> AHDC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27551448:27551448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764325293
CDS Mutation	c.668C>T
AA Mutation	p.Thr223Met(p.T223M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27548701:27548701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3415C>T
AA Mutation	p.Pro1139Ser(p.P1139S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27551766:27551766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350A>T
AA Mutation	p.Asn117Ile(p.N117I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27549199:27549199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2917G>T
AA Mutation	p.Gly973Cys(p.G973C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27552025:27552025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91G>T
AA Mutation	p.Gly31Cys(p.G31C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27549301:27549301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563439857
CDS Mutation	c.2815C>T
AA Mutation	p.Arg939Trp(p.R939W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27548304:27548304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3812C>T
AA Mutation	p.Pro1271Leu(p.P1271L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27547465:27547465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375725827
CDS Mutation	c.4651G>A
AA Mutation	p.Val1551Met(p.V1551M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27548751:27548751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3365A>G
AA Mutation	p.Glu1122Gly(p.E1122G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27548860:27548860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766744511
CDS Mutation	c.3256T>G
AA Mutation	p.Ser1086Ala(p.S1086A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27551460:27551460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773993918
CDS Mutation	c.656C>T
AA Mutation	p.Thr219Met(p.T219M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27549522:27549522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754239206
CDS Mutation	c.2594G>A
AA Mutation	p.Arg865Gln(p.R865Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27551848:27551848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776449449
CDS Mutation	c.268C>T
AA Mutation	p.Arg90Cys(p.R90C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27551991:27551991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201360711
CDS Mutation	c.125G>A
AA Mutation	p.Arg42Gln(p.R42Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27548881:27548881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371317677
CDS Mutation	c.3235A>G
AA Mutation	p.Thr1079Ala(p.T1079A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27549844:27549844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2272G>T
AA Mutation	p.Gly758Cys(p.G758C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27550068:27550068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2048C>T
AA Mutation	p.Ala683Val(p.A683V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27550494:27550494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1622T>G
AA Mutation	p.Ile541Ser(p.I541S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27551656:27551656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757919190
CDS Mutation	c.460C>T
AA Mutation	p.Arg154Cys(p.R154C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000247087
Start	27551308:27551308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808G>A
AA Mutation	p.Glu270Lys(p.E270K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247087
Start	27547808:27547808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566131872
CDS Mutation	c.4308C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247087
Start	27551585:27551585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247087
Start	27549302:27549302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2814C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247087
Start	27548546:27548546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3570A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247087
Start	27550712:27550712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1404C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247087
Start	27548351:27548351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3765C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247087
Start	27551996:27551996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247087
Start	27550475:27550475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756490904
CDS Mutation	c.1641C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247087
Start	27551921:27551921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247087
Start	27548063:27548063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769447737
CDS Mutation	c.4053G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247087
Start	27550559:27550559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777504199
CDS Mutation	c.1557G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247087
Start	27550358:27550358(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1758delA
AA Mutation	p.Lys586AsnfsTer37(p.K586Nfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247087
Start	27548981:27548981(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3135delC
AA Mutation	p.Phe1046SerfsTer96(p.F1046Sfs*96)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247087
Start	27550994:27550994(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs749294057
CDS Mutation	c.1122delC
AA Mutation	p.Pro376LeufsTer76(p.P376Lfs*76)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247087
Start	27549162:27549162(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2954delA
AA Mutation	p.Lys985SerfsTer157(p.K985Sfs*157)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247087
Start	27552017:27552017(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.99delC
AA Mutation	p.Thr34ProfsTer83(p.T34Pfs*83)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AHDC1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247087
Start	27551888:27551888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247087
Start	27550358:27550358(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1758delA
AA Mutation	p.Lys586AsnfsTer37(p.K586Nfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript