ClinVar Miner

Variants in gene DOCK8 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 45
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HGVS dbSNP gnomAD frequency
NM_203447.4(DOCK8):c.5908G>C (p.Ala1970Pro) rs34908836 0.07318
NM_203447.4(DOCK8):c.3230G>A (p.Ser1077Asn) rs34627722 0.05757
NM_203447.4(DOCK8):c.709G>A (p.Glu237Lys) rs11789099 0.02275
NM_203447.4(DOCK8):c.3840+3A>G rs16938572 0.00806
NM_203447.4(DOCK8):c.3573C>T (p.Ser1191=) rs13285348 0.00471
NM_203447.4(DOCK8):c.3701-17C>T rs376111035 0.00409
NM_203447.4(DOCK8):c.1017G>A (p.Pro339=) rs35746964 0.00360
NM_203447.4(DOCK8):c.1587C>G (p.Pro529=) rs146289269 0.00296
NM_203447.4(DOCK8):c.4019A>G (p.Tyr1340Cys) rs116920018 0.00274
NM_203447.4(DOCK8):c.1516+16C>G rs141986056 0.00266
NM_203447.4(DOCK8):c.2310G>A (p.Glu770=) rs116175117 0.00217
NM_203447.4(DOCK8):c.1582C>A (p.Leu528Met) rs146250176 0.00213
NM_203447.4(DOCK8):c.6201A>G (p.Glu2067=) rs145573166 0.00210
NM_203447.4(DOCK8):c.528+7C>A rs114833839 0.00207
NM_203447.4(DOCK8):c.4024-4C>T rs111306749 0.00196
NM_203447.4(DOCK8):c.380G>A (p.Arg127His) rs150742426 0.00189
NM_203447.4(DOCK8):c.4158C>T (p.Asn1386=) rs77803650 0.00186
NM_203447.4(DOCK8):c.3606T>C (p.Cys1202=) rs143919622 0.00175
NM_203447.4(DOCK8):c.663C>A (p.Asp221Glu) rs139391329 0.00171
NM_203447.4(DOCK8):c.3460C>T (p.Arg1154Cys) rs34390308 0.00170
NM_203447.4(DOCK8):c.640C>T (p.Leu214=) rs150446322 0.00143
NM_203447.4(DOCK8):c.5010G>A (p.Ala1670=) rs142208336 0.00128
NM_203447.4(DOCK8):c.5781C>T (p.Tyr1927=) rs138225192 0.00122
NM_203447.4(DOCK8):c.3813A>G (p.Lys1271=) rs75411647 0.00115
NM_203447.4(DOCK8):c.1881T>C (p.Phe627=) rs140134223 0.00095
NM_203447.4(DOCK8):c.3841-11C>T rs372829200 0.00089
NM_203447.4(DOCK8):c.4588C>G (p.Leu1530Val) rs536373496 0.00084
NM_203447.4(DOCK8):c.3988C>G (p.Leu1330Val) rs148081681 0.00076
NM_203447.4(DOCK8):c.1422+17C>T rs200839477 0.00071
NM_203447.4(DOCK8):c.5962-8C>T rs749575443 0.00061
NM_203447.4(DOCK8):c.3058A>G (p.Ile1020Val) rs151094543 0.00046
NM_203447.4(DOCK8):c.5355+6C>T rs188141951 0.00046
NM_203447.4(DOCK8):c.828-7A>G rs200243583 0.00030
NM_203447.4(DOCK8):c.470C>T (p.Thr157Met) rs575314722 0.00011
NM_203447.4(DOCK8):c.3079G>A (p.Val1027Ile) rs199782622 0.00009
NM_203447.4(DOCK8):c.2646G>A (p.Thr882=) rs373515697 0.00005
NM_203447.4(DOCK8):c.2778+20G>A rs587780923 0.00005
NM_203447.4(DOCK8):c.3234+15_3234+16delinsAC rs2131416494
NM_203447.4(DOCK8):c.3234+15del rs375864618
NM_203447.4(DOCK8):c.53+14del rs749863710
NM_203447.4(DOCK8):c.5962-13_5962-9del rs35071801
NM_203447.4(DOCK8):c.5962-16_5962-9del rs35071801
NM_203447.4(DOCK8):c.5962-17_5962-9del rs35071801
NM_203447.4(DOCK8):c.5962-19_5962-9del rs35071801
NM_203447.4(DOCK8):c.5962-34_5962-26del rs747332634

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