ClinVar Miner

List of variants in gene combination INSRR, NTRK1 reported as likely benign for not provided

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Gene type:
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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_014215.3(INSRR):c.3237+45C>G rs13376034 0.01497
NM_014215.3(INSRR):c.3397+98G>C rs79020702 0.00516
NM_014215.3(INSRR):c.789G>A (p.Pro263=) rs138142163 0.00219
NM_014215.3(INSRR):c.1660C>T (p.Arg554Cys) rs56068937 0.00199
NM_014215.3(INSRR):c.736T>C (p.Cys246Arg) rs56377825 0.00197
NM_014215.3(INSRR):c.879C>T (p.Phe293=) rs55881234 0.00107
NM_014215.3(INSRR):c.1215C>T (p.Asp405=) rs141373320 0.00098
NM_014215.3(INSRR):c.3513C>T (p.Thr1171=) rs55694053 0.00068
NM_014215.3(INSRR):c.2250C>T (p.Pro750=) rs141332542 0.00052
NM_014215.3(INSRR):c.835C>T (p.Arg279Cys) rs150841787 0.00019
NM_014215.3(INSRR):c.775C>T (p.Leu259=) rs148794008 0.00012
NM_014215.3(INSRR):c.259C>T (p.Arg87Cys) rs374390533 0.00009
NM_014215.3(INSRR):c.3265T>C (p.Leu1089=) rs150557473 0.00009
NM_014215.3(INSRR):c.2796G>A (p.Thr932=) rs775750741 0.00006
NM_014215.3(INSRR):c.1785C>T (p.Ile595=) rs537871557 0.00003
NM_014215.3(INSRR):c.2700T>G (p.Ser900=) rs762614947 0.00001
NM_014215.3(INSRR):c.1020G>A (p.Ala340=)
NM_014215.3(INSRR):c.1786G>A (p.Val596Ile)
NM_014215.3(INSRR):c.201C>T (p.Asp67=)
NM_014215.3(INSRR):c.2454T>A (p.Ile818=) rs761205184
NM_014215.3(INSRR):c.285C>T (p.Arg95=)
NM_014215.3(INSRR):c.3042G>A (p.Thr1014=)
NM_014215.3(INSRR):c.3339C>T (p.His1113=)
NM_014215.3(INSRR):c.3789G>A (p.Pro1263=) rs370144321
NM_014215.3(INSRR):c.380C>A (p.Ala127Glu)
NM_014215.3(INSRR):c.534C>T (p.Asp178=)
NM_014215.3(INSRR):c.56C>T (p.Ser19Phe)

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