Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ANKRD17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73135251:73135251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771330970
CDS Mutation	c.3100G>A
AA Mutation	p.Ala1034Thr(p.A1034T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73140015:73140015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2601G>T
AA Mutation	p.Glu867Asp(p.E867D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73135158:73135158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3193G>A
AA Mutation	p.Ala1065Thr(p.A1065T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73091737:73091737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5891C>A
AA Mutation	p.Ser1964Tyr(p.S1964Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73121708:73121708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3544T>G
AA Mutation	p.Ser1182Ala(p.S1182A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73121710:73121710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3542T>G
AA Mutation	p.Val1181Gly(p.V1181G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73139728:73139728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2888C>A
AA Mutation	p.Pro963His(p.P963H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73258352:73258352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317G>A
AA Mutation	p.Gly106Asp(p.G106D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73098211:73098211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4883A>G
AA Mutation	p.Asn1628Ser(p.N1628S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73098161:73098161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4933A>G
AA Mutation	p.Thr1645Ala(p.T1645A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73153985:73153985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1129G>A
AA Mutation	p.Ala377Thr(p.A377T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73091786:73091786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5842C>T
AA Mutation	p.Arg1948Cys(p.R1948C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73078750:73078750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143161842
CDS Mutation	c.7300C>T
AA Mutation	p.Arg2434Cys(p.R2434C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73142269:73142269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2202A>T
AA Mutation	p.Leu734Phe(p.L734F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73091785:73091785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5843G>A
AA Mutation	p.Arg1948His(p.R1948H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73094152:73094152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5254C>T
AA Mutation	p.Arg1752Trp(p.R1752W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73139932:73139932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2684G>T
AA Mutation	p.Arg895Ile(p.R895I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73135131:73135131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3220G>T
AA Mutation	p.Asp1074Tyr(p.D1074Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73102512:73102512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372433463
CDS Mutation	c.4437G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73147395:73147395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1605A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73153974:73153974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769329051
CDS Mutation	c.1140G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73085427:73085427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6981G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73092168:73092168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5460A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73258348:73258348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73139712:73139712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2904C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73146806:73146806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773274616
CDS Mutation	c.1827T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73091952:73091952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5676T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73091130:73091130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6498C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73098267:73098267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779070522
CDS Mutation	c.4827C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73078730:73078730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746041277
CDS Mutation	c.7320G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358602
Start	73090884:73090884(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6744delC
AA Mutation	p.Leu2249TyrfsTer84(p.L2249Yfs*84)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358602
Start	73139959:73139959(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2657delA
AA Mutation	p.Lys886SerfsTer4(p.K886Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000358602
Start	73148840:73148840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1540G>T
AA Mutation	p.Glu514Ter(p.E514*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000358602
Start	73140137:73140137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2479G>T
AA Mutation	p.Glu827Ter(p.E827*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ANKRD17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73120961:73120961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3769A>G
AA Mutation	p.Thr1257Ala(p.T1257A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73118692:73118692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4184G>T
AA Mutation	p.Arg1395Ile(p.R1395I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73147319:73147319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1681G>A
AA Mutation	p.Glu561Lys(p.E561K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73142352:73142352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2119G>A
AA Mutation	p.Gly707Ser(p.G707S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73092155:73092155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5473A>C
AA Mutation	p.Thr1825Pro(p.T1825P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358602
Start	73098269:73098269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4825A>C
AA Mutation	p.Ser1609Arg(p.S1609R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358602
Start	73091517:73091517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000358602
Start	73139681:73139681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2935G>T
AA Mutation	p.Glu979Ter(p.E979*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000358602
Start	73120895:73120895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3835G>T
AA Mutation	p.Glu1279Ter(p.E1279*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript