ClinVar Miner

List of variants in gene PIEZO2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_001378183.1(PIEZO2):c.7326C>T (p.Tyr2442=) rs72970080 0.00237
NM_001378183.1(PIEZO2):c.5378C>G (p.Thr1793Arg) rs186065260 0.00220
NM_001378183.1(PIEZO2):c.8340C>T (p.Gly2780=) rs146400447 0.00192
NM_001378183.1(PIEZO2):c.5355C>T (p.Pro1785=) rs191626967 0.00178
NM_001378183.1(PIEZO2):c.6013G>A (p.Asp2005Asn) rs199842060 0.00170
NM_001378183.1(PIEZO2):c.2595G>A (p.Pro865=) rs372274945 0.00108
NM_001378183.1(PIEZO2):c.8268G>A (p.Pro2756=) rs138454862 0.00101
NM_001378183.1(PIEZO2):c.6153C>T (p.Ala2051=) rs375812718 0.00072
NM_001378183.1(PIEZO2):c.5502A>C (p.Thr1834=) rs543259433 0.00066
NM_001378183.1(PIEZO2):c.2964T>C (p.Tyr988=) rs200998919 0.00045
NM_001378183.1(PIEZO2):c.948G>A (p.Thr316=) rs372688364 0.00029
NM_001378183.1(PIEZO2):c.5982C>T (p.Ser1994=) rs377649969 0.00026
NM_001378183.1(PIEZO2):c.7317C>T (p.Ser2439=) rs754942478 0.00026
NM_001378183.1(PIEZO2):c.6207C>T (p.Ser2069=) rs776951650 0.00025
NM_001378183.1(PIEZO2):c.751T>C (p.Leu251=) rs773154803 0.00020
NM_001378183.1(PIEZO2):c.1170C>T (p.Tyr390=) rs201658108 0.00010
NM_001378183.1(PIEZO2):c.474G>A (p.Glu158=) rs369019214 0.00009
NM_001378183.1(PIEZO2):c.1941A>C (p.Glu647Asp) rs1021262669 0.00006
NM_001378183.1(PIEZO2):c.3201A>T (p.Thr1067=) rs552989428 0.00003
NM_001378183.1(PIEZO2):c.3561C>T (p.Ile1187=) rs370577821 0.00003
NM_001378183.1(PIEZO2):c.5871G>A (p.Ser1957=) rs776642495 0.00003
NM_001378183.1(PIEZO2):c.6630G>A (p.Lys2210=) rs781075542 0.00003
NM_001378183.1(PIEZO2):c.8034C>T (p.Ile2678=) rs376582837 0.00002
NM_001378183.1(PIEZO2):c.6354C>T (p.Asn2118=) rs1200814977 0.00001
NM_001378183.1(PIEZO2):c.1261G>C (p.Gly421Arg) rs202104395
NM_001378183.1(PIEZO2):c.1867G>A (p.Glu623Lys) rs1555647548
NM_001378183.1(PIEZO2):c.2490C>T (p.Tyr830=)
NM_001378183.1(PIEZO2):c.2626C>T (p.Leu876=) rs2510697246
NM_001378183.1(PIEZO2):c.2997G>A (p.Pro999=) rs188464402
NM_001378183.1(PIEZO2):c.3261G>C (p.Leu1087=) rs866552884
NM_001378183.1(PIEZO2):c.3534C>G (p.Val1178=)
NM_001378183.1(PIEZO2):c.48C>T (p.Pro16=)
NM_001378183.1(PIEZO2):c.5598G>C (p.Thr1866=) rs78023192
NM_001378183.1(PIEZO2):c.5916C>T (p.Asp1972=) rs529388684
NM_001378183.1(PIEZO2):c.8467T>C (p.Leu2823=) rs1274299783
NM_001378183.1(PIEZO2):c.900C>T (p.Pro300=) rs1458950572

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