ClinVar Miner

Variants in gene TRRAP with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 32
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HGVS dbSNP gnomAD frequency
NM_001375524.1(TRRAP):c.1809T>C (p.Tyr603=) rs34648627 0.00556
NM_001375524.1(TRRAP):c.6213C>G (p.Ala2071=) rs140869162 0.00299
NM_001375524.1(TRRAP):c.7644T>C (p.His2548=) rs144017858 0.00186
NM_001375524.1(TRRAP):c.1962G>A (p.Thr654=) rs34964388 0.00174
NM_001375524.1(TRRAP):c.1905C>T (p.Phe635=) rs149527392 0.00137
NM_001375524.1(TRRAP):c.1563G>A (p.Pro521=) rs145259394 0.00111
NM_001375524.1(TRRAP):c.1115+6A>C rs202033080 0.00060
NM_001375524.1(TRRAP):c.6972C>T (p.Thr2324=) rs143292301 0.00044
NM_001375524.1(TRRAP):c.6381G>A (p.Glu2127=) rs146661901 0.00029
NM_001375524.1(TRRAP):c.634-3C>T rs113339948 0.00024
NM_001375524.1(TRRAP):c.2087G>A (p.Arg696His) rs200324989 0.00021
NM_001375524.1(TRRAP):c.11191G>A (p.Ala3731Thr) rs199541716 0.00011
NM_001375524.1(TRRAP):c.6872G>A (p.Ser2291Asn) rs199827128 0.00008
NM_001375524.1(TRRAP):c.511C>T (p.Arg171Cys) rs200157211 0.00003
NM_001375524.1(TRRAP):c.4405-5A>G rs782409632 0.00002
NM_001375524.1(TRRAP):c.10512G>A (p.Thr3504=)
NM_001375524.1(TRRAP):c.11088G>A (p.Ala3696=)
NM_001375524.1(TRRAP):c.2108A>G (p.Asn703Ser)
NM_001375524.1(TRRAP):c.2601G>A (p.Pro867=)
NM_001375524.1(TRRAP):c.3592-6T>A
NM_001375524.1(TRRAP):c.4161C>T (p.Ile1387=)
NM_001375524.1(TRRAP):c.4671G>A (p.Ala1557=)
NM_001375524.1(TRRAP):c.4809C>T (p.Asp1603=)
NM_001375524.1(TRRAP):c.4900G>A (p.Gly1634Ser)
NM_001375524.1(TRRAP):c.6977-4G>A
NM_001375524.1(TRRAP):c.8207C>T (p.Thr2736Met)
NM_001375524.1(TRRAP):c.8274T>C (p.Leu2758=)
NM_001375524.1(TRRAP):c.8355T>A (p.Ile2785=)
NM_001375524.1(TRRAP):c.8625G>A (p.Ala2875=)
NM_001375524.1(TRRAP):c.9262G>A (p.Val3088Ile)
NM_001375524.1(TRRAP):c.9288+4C>A
NM_001375524.1(TRRAP):c.9780G>A (p.Ala3260=)

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