ClinVar Miner

List of variants in gene PHIP reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 154
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HGVS dbSNP gnomAD frequency
NM_017934.7(PHIP):c.2256G>A (p.Arg752=) rs149171291 0.00225
NM_017934.7(PHIP):c.1563A>G (p.Lys521=) rs142963281 0.00118
NM_017934.7(PHIP):c.2538-8C>G rs369962833 0.00019
NM_017934.7(PHIP):c.2667A>T (p.Lys889Asn) rs756471447 0.00006
NM_017934.7(PHIP):c.499A>G (p.Thr167Ala) rs748247534 0.00005
NM_017934.7(PHIP):c.2058C>T (p.Asn686=) rs374059830 0.00004
NM_017934.7(PHIP):c.923+3C>A rs747091686 0.00001
NM_017934.7(PHIP):c.100-14C>G
NM_017934.7(PHIP):c.100-16C>T
NM_017934.7(PHIP):c.100-18C>T
NM_017934.7(PHIP):c.100-4G>A
NM_017934.7(PHIP):c.1006C>T (p.Leu336=)
NM_017934.7(PHIP):c.1011G>A (p.Ala337=)
NM_017934.7(PHIP):c.1095+8T>C
NM_017934.7(PHIP):c.1096-16_1096-13del
NM_017934.7(PHIP):c.1136+14C>G
NM_017934.7(PHIP):c.1137-19C>T
NM_017934.7(PHIP):c.1137-5T>C
NM_017934.7(PHIP):c.1161G>C (p.Gly387=)
NM_017934.7(PHIP):c.1179A>G (p.Gln393=)
NM_017934.7(PHIP):c.1202G>A (p.Ser401Asn)
NM_017934.7(PHIP):c.1235+8G>T
NM_017934.7(PHIP):c.1236-12C>A
NM_017934.7(PHIP):c.1242C>T (p.Asn414=)
NM_017934.7(PHIP):c.1251A>G (p.Gly417=)
NM_017934.7(PHIP):c.129+12_129+42del rs2127784613
NM_017934.7(PHIP):c.129+13G>A
NM_017934.7(PHIP):c.129+7G>T
NM_017934.7(PHIP):c.129+8C>T
NM_017934.7(PHIP):c.129+9G>A
NM_017934.7(PHIP):c.130-10C>G
NM_017934.7(PHIP):c.130-12C>T
NM_017934.7(PHIP):c.130-13C>T
NM_017934.7(PHIP):c.130-17G>T
NM_017934.7(PHIP):c.130-4G>T
NM_017934.7(PHIP):c.130-5C>T
NM_017934.7(PHIP):c.130-8C>A
NM_017934.7(PHIP):c.1312A>G (p.Thr438Ala)
NM_017934.7(PHIP):c.1362C>T (p.Tyr454=)
NM_017934.7(PHIP):c.1389+19C>T
NM_017934.7(PHIP):c.1390-20A>G
NM_017934.7(PHIP):c.1431C>T (p.Phe477=)
NM_017934.7(PHIP):c.1488G>A (p.Leu496=)
NM_017934.7(PHIP):c.150C>T (p.Asp50=)
NM_017934.7(PHIP):c.1524+9_1524+11del
NM_017934.7(PHIP):c.1545C>A (p.Gly515=)
NM_017934.7(PHIP):c.1545C>T (p.Gly515=)
NM_017934.7(PHIP):c.1569T>C (p.Ser523=)
NM_017934.7(PHIP):c.1608A>G (p.Gly536=)
NM_017934.7(PHIP):c.1629T>C (p.Phe543=)
NM_017934.7(PHIP):c.1653+11A>G
NM_017934.7(PHIP):c.1653+8A>T
NM_017934.7(PHIP):c.1653+9T>G
NM_017934.7(PHIP):c.1662T>C (p.Asp554=)
NM_017934.7(PHIP):c.1692A>C (p.Pro564=)
NM_017934.7(PHIP):c.1707C>G (p.Ala569=)
NM_017934.7(PHIP):c.1746T>G (p.Pro582=)
NM_017934.7(PHIP):c.1779T>C (p.Val593=)
NM_017934.7(PHIP):c.1806T>C (p.Tyr602=)
NM_017934.7(PHIP):c.1815A>G (p.Leu605=)
NM_017934.7(PHIP):c.1848A>G (p.Gln616=)
NM_017934.7(PHIP):c.1879+10C>T
NM_017934.7(PHIP):c.1880-16G>C
NM_017934.7(PHIP):c.1880-19T>C
NM_017934.7(PHIP):c.1880-4A>G
NM_017934.7(PHIP):c.1950A>G (p.Leu650=)
NM_017934.7(PHIP):c.1953A>G (p.Gln651=)
NM_017934.7(PHIP):c.1965C>T (p.Asp655=)
NM_017934.7(PHIP):c.1979G>T (p.Gly660Val)
NM_017934.7(PHIP):c.2040G>A (p.Glu680=)
NM_017934.7(PHIP):c.2040G>C (p.Glu680Asp)
NM_017934.7(PHIP):c.2067A>G (p.Leu689=)
NM_017934.7(PHIP):c.2068A>C (p.Arg690=)
NM_017934.7(PHIP):c.2076T>C (p.Ser692=)
NM_017934.7(PHIP):c.2100A>G (p.Gln700=)
NM_017934.7(PHIP):c.2106C>T (p.His702=)
NM_017934.7(PHIP):c.2136A>G (p.Thr712=)
NM_017934.7(PHIP):c.2139G>A (p.Glu713=)
NM_017934.7(PHIP):c.216T>C (p.Pro72=)
NM_017934.7(PHIP):c.2190T>C (p.Ala730=)
NM_017934.7(PHIP):c.2196A>C (p.Val732=)
NM_017934.7(PHIP):c.2202-14C>A
NM_017934.7(PHIP):c.2202-18_2202-17del
NM_017934.7(PHIP):c.2202-7C>A
NM_017934.7(PHIP):c.2254A>G (p.Arg752Gly)
NM_017934.7(PHIP):c.2304A>G (p.Ile768Met) rs1064796425
NM_017934.7(PHIP):c.2313C>T (p.Val771=)
NM_017934.7(PHIP):c.2320-16_2320-12del
NM_017934.7(PHIP):c.2382C>T (p.His794=)
NM_017934.7(PHIP):c.2442T>C (p.Asn814=)
NM_017934.7(PHIP):c.2460+20A>G
NM_017934.7(PHIP):c.2461-10C>T
NM_017934.7(PHIP):c.2461-5C>T
NM_017934.7(PHIP):c.2466C>T (p.Gly822=)
NM_017934.7(PHIP):c.2496C>G (p.Ser832=)
NM_017934.7(PHIP):c.2496C>T (p.Ser832=) rs376565558
NM_017934.7(PHIP):c.2499A>G (p.Glu833=)
NM_017934.7(PHIP):c.2537+11G>A
NM_017934.7(PHIP):c.2537+18A>C
NM_017934.7(PHIP):c.255T>C (p.Leu85=)
NM_017934.7(PHIP):c.2598A>G (p.Pro866=)
NM_017934.7(PHIP):c.2615A>G (p.Asn872Ser)
NM_017934.7(PHIP):c.2715A>G (p.Glu905=)
NM_017934.7(PHIP):c.2743A>G (p.Lys915Glu)
NM_017934.7(PHIP):c.2769+13A>G
NM_017934.7(PHIP):c.2769+15A>G
NM_017934.7(PHIP):c.321T>A (p.Ser107=)
NM_017934.7(PHIP):c.327A>G (p.Leu109=)
NM_017934.7(PHIP):c.340+17A>G
NM_017934.7(PHIP):c.340+4T>A
NM_017934.7(PHIP):c.381G>A (p.Ala127=)
NM_017934.7(PHIP):c.41-13C>G
NM_017934.7(PHIP):c.41-13C>T
NM_017934.7(PHIP):c.41-15C>T
NM_017934.7(PHIP):c.41-17C>T
NM_017934.7(PHIP):c.41-6G>A
NM_017934.7(PHIP):c.41-7C>T
NM_017934.7(PHIP):c.41-8C>T
NM_017934.7(PHIP):c.414T>A (p.Val138=)
NM_017934.7(PHIP):c.429A>C (p.Pro143=)
NM_017934.7(PHIP):c.439+14G>A
NM_017934.7(PHIP):c.440-13T>C
NM_017934.7(PHIP):c.440-14C>G
NM_017934.7(PHIP):c.477C>T (p.Tyr159=)
NM_017934.7(PHIP):c.478A>C (p.Arg160=)
NM_017934.7(PHIP):c.504A>G (p.Ala168=)
NM_017934.7(PHIP):c.510T>C (p.Tyr170=)
NM_017934.7(PHIP):c.51C>T (p.Phe17=) rs778180694
NM_017934.7(PHIP):c.54C>T (p.Leu18=)
NM_017934.7(PHIP):c.57C>T (p.Ile19=)
NM_017934.7(PHIP):c.600+13T>A
NM_017934.7(PHIP):c.600+14A>G
NM_017934.7(PHIP):c.601-19T>C
NM_017934.7(PHIP):c.601-4T>C rs202141638
NM_017934.7(PHIP):c.601-8A>T
NM_017934.7(PHIP):c.603T>C (p.Gly201=)
NM_017934.7(PHIP):c.63G>C (p.Arg21=)
NM_017934.7(PHIP):c.657T>G (p.Ala219=)
NM_017934.7(PHIP):c.66C>T (p.Phe22=)
NM_017934.7(PHIP):c.696T>C (p.Ala232=)
NM_017934.7(PHIP):c.70G>C (p.Glu24Gln)
NM_017934.7(PHIP):c.738T>C (p.Asp246=)
NM_017934.7(PHIP):c.741A>G (p.Lys247=)
NM_017934.7(PHIP):c.90G>A (p.Gln30=)
NM_017934.7(PHIP):c.923+20C>T
NM_017934.7(PHIP):c.923+3C>G
NM_017934.7(PHIP):c.924-16A>G
NM_017934.7(PHIP):c.924-7A>T
NM_017934.7(PHIP):c.951C>A (p.Arg317=)
NM_017934.7(PHIP):c.97C>G (p.Gln33Glu)
NM_017934.7(PHIP):c.99+14_99+20del
NM_017934.7(PHIP):c.99+15G>A
NM_017934.7(PHIP):c.99+19C>G
NM_017934.7(PHIP):c.995-14G>A

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