ClinVar Miner

List of variants in gene PTPN11 reported as likely benign for Cardiovascular phenotype

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Total variants: 10
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HGVS dbSNP
NM_002834.4(PTPN11):c.1404G>A (p.Thr468=) rs587781130
NM_002834.4(PTPN11):c.1449T>G (p.Gly483=) rs143238917
NM_002834.4(PTPN11):c.162C>T (p.Ile54=) rs1207829516
NM_002834.4(PTPN11):c.1650G>A (p.Ala550=) rs374896287
NM_002834.4(PTPN11):c.1658C>T (p.Thr553Met) rs148176616
NM_002834.4(PTPN11):c.1746C>T (p.Asn582=) rs397516800
NM_002834.4(PTPN11):c.426C>T (p.Ser142=) rs199498784
NM_002834.4(PTPN11):c.486C>T (p.Asp162=) rs397507522
NM_002834.4(PTPN11):c.558G>T (p.Arg186=) rs200920312
NM_002834.4(PTPN11):c.874C>T (p.Leu292=) rs930267460

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