List of variants in gene ANKRD26 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 45

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HGVS	dbSNP	gnomAD frequency
NM_014915.3(ANKRD26):c.2679A>G (p.Gln893=)	rs61730098	0.00215
NM_014915.3(ANKRD26):c.3007G>A (p.Glu1003Lys)	rs41304587	0.00141
NM_014915.3(ANKRD26):c.542C>T (p.Thr181Ile)	rs191015656	0.00093
NM_014915.3(ANKRD26):c.3735G>A (p.Thr1245=)	rs199716344	0.00079
NM_014915.3(ANKRD26):c.1998A>G (p.Lys666=)	rs372489280	0.00052
NM_014915.3(ANKRD26):c.945A>G (p.Gln315=)	rs200199151	0.00052
NM_014915.3(ANKRD26):c.4188T>C (p.Asp1396=)	rs199589035	0.00046
NM_014915.3(ANKRD26):c.679C>T (p.Pro227Ser)	rs201638257	0.00039
NM_014915.3(ANKRD26):c.2855A>C (p.Lys952Thr)	rs564448342	0.00035
NM_014915.3(ANKRD26):c.1728T>C (p.Asp576=)	rs200379534	0.00031
NM_014915.3(ANKRD26):c.599A>G (p.Lys200Arg)	rs150623081	0.00031
NM_014915.3(ANKRD26):c.1970A>T (p.Asp657Val)	rs193178384	0.00027
NM_014915.3(ANKRD26):c.3761A>G (p.Asp1254Gly)	rs368705077	0.00024
NM_014915.3(ANKRD26):c.874+8G>T	rs377114195	0.00023
NM_014915.3(ANKRD26):c.-117G>A	rs560384691	0.00011
NM_014915.3(ANKRD26):c.301G>A (p.Asp101Asn)	rs199753643	0.00007
NM_014915.3(ANKRD26):c.3286C>T (p.Arg1096Trp)	rs367849518	0.00007
NM_014915.3(ANKRD26):c.-135A>G
NM_014915.3(ANKRD26):c.-164C>T
NM_014915.3(ANKRD26):c.1116T>C (p.Asn372=)
NM_014915.3(ANKRD26):c.1269+7_1269+12delinsA	rs386742210
NM_014915.3(ANKRD26):c.1364-5C>A
NM_014915.3(ANKRD26):c.1364A>G (p.Asp455Gly)	rs199857139
NM_014915.3(ANKRD26):c.1462+4del
NM_014915.3(ANKRD26):c.1565-4dup
NM_014915.3(ANKRD26):c.1611A>G (p.Glu537=)
NM_014915.3(ANKRD26):c.1867C>T (p.Arg623Trp)
NM_014915.3(ANKRD26):c.2053G>A (p.Asp685Asn)
NM_014915.3(ANKRD26):c.2161+6del
NM_014915.3(ANKRD26):c.2403G>A (p.Lys801=)
NM_014915.3(ANKRD26):c.240C>T (p.Asn80=)
NM_014915.3(ANKRD26):c.2421G>A (p.Thr807=)
NM_014915.3(ANKRD26):c.2562C>T (p.Val854=)
NM_014915.3(ANKRD26):c.2778A>G (p.Leu926=)
NM_014915.3(ANKRD26):c.333C>T (p.Asn111=)
NM_014915.3(ANKRD26):c.3705A>G (p.Gln1235=)
NM_014915.3(ANKRD26):c.371A>T (p.Gln124Leu)	rs200100926
NM_014915.3(ANKRD26):c.4077G>A (p.Glu1359=)
NM_014915.3(ANKRD26):c.4098C>T (p.Leu1366=)
NM_014915.3(ANKRD26):c.4128A>G (p.Glu1376=)
NM_014915.3(ANKRD26):c.4707G>A (p.Leu1569=)
NM_014915.3(ANKRD26):c.4954-4dup
NM_014915.3(ANKRD26):c.5124T>C (p.Tyr1708=)
NM_014915.3(ANKRD26):c.937G>T (p.Asp313Tyr)	rs61730102
NM_014915.3(ANKRD26):c.948T>C (p.Asp316=)	rs569751156

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