ClinVar Miner

List of variants in gene MTAP reported as uncertain significance for connective tissue neoplasm

Included ClinVar conditions (122):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP
NM_002451.4(MTAP):c.*102A>G rs755040797
NM_002451.4(MTAP):c.*1093G>T
NM_002451.4(MTAP):c.*1140A>G rs886063785
NM_002451.4(MTAP):c.*1197C>G rs886063786
NM_002451.4(MTAP):c.*1384G>C rs755911467
NM_002451.4(MTAP):c.*1399C>A
NM_002451.4(MTAP):c.*1453C>T
NM_002451.4(MTAP):c.*1482A>G rs560361151
NM_002451.4(MTAP):c.*1558G>C
NM_002451.4(MTAP):c.*1608del rs886063787
NM_002451.4(MTAP):c.*1621_*1622del rs11358276
NM_002451.4(MTAP):c.*1668T>C
NM_002451.4(MTAP):c.*1760A>G rs886063788
NM_002451.4(MTAP):c.*1831T>A rs886063789
NM_002451.4(MTAP):c.*1836C>G
NM_002451.4(MTAP):c.*2033G>A
NM_002451.4(MTAP):c.*2111A>G
NM_002451.4(MTAP):c.*2171G>A rs886063790
NM_002451.4(MTAP):c.*2183T>C
NM_002451.4(MTAP):c.*2269A>T
NM_002451.4(MTAP):c.*2286A>G
NM_002451.4(MTAP):c.*2333C>G
NM_002451.4(MTAP):c.*2383C>T rs886063791
NM_002451.4(MTAP):c.*2481T>C
NM_002451.4(MTAP):c.*254A>T
NM_002451.4(MTAP):c.*258del rs886063782
NM_002451.4(MTAP):c.*2606G>C rs886063792
NM_002451.4(MTAP):c.*2638G>A rs556394357
NM_002451.4(MTAP):c.*2651G>A rs569725867
NM_002451.4(MTAP):c.*2660C>A
NM_002451.4(MTAP):c.*2693G>A
NM_002451.4(MTAP):c.*2740G>A
NM_002451.4(MTAP):c.*2837T>A rs566068002
NM_002451.4(MTAP):c.*2912G>C rs775831366
NM_002451.4(MTAP):c.*2937C>G
NM_002451.4(MTAP):c.*2968T>C rs554780978
NM_002451.4(MTAP):c.*303G>A
NM_002451.4(MTAP):c.*3052C>T rs182636316
NM_002451.4(MTAP):c.*3057T>A
NM_002451.4(MTAP):c.*3060A>G
NM_002451.4(MTAP):c.*3072G>A rs768885564
NM_002451.4(MTAP):c.*3160T>C
NM_002451.4(MTAP):c.*3206C>T rs886063793
NM_002451.4(MTAP):c.*3276A>G
NM_002451.4(MTAP):c.*3361C>T rs138870323
NM_002451.4(MTAP):c.*3389T>C rs765432220
NM_002451.4(MTAP):c.*3501T>C
NM_002451.4(MTAP):c.*3656A>G
NM_002451.4(MTAP):c.*3692G>A
NM_002451.4(MTAP):c.*3766C>T rs149649469
NM_002451.4(MTAP):c.*3774A>G
NM_002451.4(MTAP):c.*378T>C rs886063783
NM_002451.4(MTAP):c.*3943G>A rs886063794
NM_002451.4(MTAP):c.*395A>G
NM_002451.4(MTAP):c.*730A>G
NM_002451.4(MTAP):c.*795A>T
NM_002451.4(MTAP):c.*912A>G
NM_002451.4(MTAP):c.-108_-103del rs886063780
NM_002451.4(MTAP):c.-52G>C
NM_002451.4(MTAP):c.119A>G (p.Lys40Arg)
NM_002451.4(MTAP):c.187A>G (p.Arg63Gly) rs886063781
NM_002451.4(MTAP):c.224A>G (p.Gln75Arg)
NM_002451.4(MTAP):c.300G>A (p.Glu100=) rs762121645
NM_002451.4(MTAP):c.572C>T (p.Ala191Val) rs200708704

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