ClinVar Miner

List of variants in gene combination LOC126806421, TTN reported as uncertain significance by Revvity Omics, Revvity

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Total variants: 31
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HGVS dbSNP gnomAD frequency
NM_001267550.2(TTN):c.96928A>C (p.Thr32310Pro) rs542208825 0.00018
NM_001267550.2(TTN):c.96173G>A (p.Arg32058Gln) rs374063064 0.00014
NM_001267550.2(TTN):c.96904+4T>C rs373514079 0.00014
NM_001267550.2(TTN):c.96172C>T (p.Arg32058Trp) rs201463708 0.00008
NM_001267550.2(TTN):c.96883G>A (p.Val32295Met) rs199532781 0.00007
NM_001267550.2(TTN):c.96424G>A (p.Val32142Ile) rs779663332 0.00006
NM_001267550.2(TTN):c.96526T>A (p.Tyr32176Asn) rs377291343 0.00006
NM_001267550.2(TTN):c.96637G>A (p.Asp32213Asn) rs764561909 0.00006
NM_001267550.2(TTN):c.96286G>A (p.Ala32096Thr) rs376039623 0.00005
NM_001267550.2(TTN):c.96140C>T (p.Thr32047Met) rs375640847 0.00004
NM_001267550.2(TTN):c.96644C>G (p.Thr32215Ser) rs975713554 0.00003
NM_001267550.2(TTN):c.96934C>T (p.Pro32312Ser) rs1024823449 0.00003
NM_001267550.2(TTN):c.96604G>T (p.Val32202Leu) rs755717335 0.00002
NM_001267550.2(TTN):c.96685G>A (p.Asp32229Asn) rs770101398 0.00001
NM_001267550.2(TTN):c.96698G>A (p.Arg32233Gln) rs755082341 0.00001
NM_001267550.2(TTN):c.96049G>A (p.Ala32017Thr)
NM_001267550.2(TTN):c.96125C>T (p.Pro32042Leu)
NM_001267550.2(TTN):c.96212T>G (p.Ile32071Arg) rs755545981
NM_001267550.2(TTN):c.96235G>A (p.Asp32079Asn) rs200540781
NM_001267550.2(TTN):c.96235G>C (p.Asp32079His) rs200540781
NM_001267550.2(TTN):c.96356G>A (p.Arg32119Lys)
NM_001267550.2(TTN):c.96413A>T (p.Asn32138Ile)
NM_001267550.2(TTN):c.96503G>A (p.Gly32168Glu)
NM_001267550.2(TTN):c.96574G>A (p.Glu32192Lys)
NM_001267550.2(TTN):c.96599C>T (p.Ser32200Leu)
NM_001267550.2(TTN):c.96803A>G (p.Asn32268Ser)
NM_001267550.2(TTN):c.96830T>A (p.Ile32277Lys)
NM_001267550.2(TTN):c.96854T>C (p.Val32285Ala)
NM_001267550.2(TTN):c.96868G>A (p.Glu32290Lys) rs1060500512
NM_001267550.2(TTN):c.96919G>A (p.Asp32307Asn)
NM_001267550.2(TTN):c.96947T>C (p.Ile32316Thr)

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