ClinVar Miner

List of variants studied for cleft palate by Illumina Clinical Services Laboratory,Illumina

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_001109878.2(TBX22):c.*293T>C
NM_001109878.2(TBX22):c.*347T>C rs142483621
NM_001109878.2(TBX22):c.*533A>T rs770782241
NM_001109878.2(TBX22):c.*57A>T rs1057515991
NM_001109878.2(TBX22):c.*6C>A rs137881052
NM_001109878.2(TBX22):c.*97C>A rs757571902
NM_001109878.2(TBX22):c.-103G>A rs73496511
NM_001109878.2(TBX22):c.-2-7C>A rs185298778
NM_001109878.2(TBX22):c.-23A>G rs147593294
NM_001109878.2(TBX22):c.-28G>A rs746947861
NM_001109878.2(TBX22):c.1090C>T (p.Leu364=) rs147281246
NM_001109878.2(TBX22):c.1169C>A (p.Ala390Asp)
NM_001109878.2(TBX22):c.1412C>T (p.Ser471Phe) rs1057515990
NM_001109878.2(TBX22):c.143G>A (p.Arg48Lys)
NM_001109878.2(TBX22):c.1488C>T (p.Asp496=) rs35602350
NM_001109878.2(TBX22):c.1544C>A (p.Ala515Glu) rs201336957
NM_001109878.2(TBX22):c.176-13C>A rs55760411
NM_001109878.2(TBX22):c.224G>T (p.Gly75Val)
NM_001109878.2(TBX22):c.240C>T (p.Tyr80=)
NM_001109878.2(TBX22):c.302T>A (p.Leu101Gln)
NM_001109878.2(TBX22):c.356+6G>C
NM_001109878.2(TBX22):c.549C>G (p.Pro183=)
NM_001109878.2(TBX22):c.554C>T (p.Ser185Leu) rs765734398
NM_001109878.2(TBX22):c.559G>A (p.Glu187Lys) rs34244923
NM_001109878.2(TBX22):c.72C>T (p.Leu24=) rs138387312
NM_001109878.2(TBX22):c.798+11T>C rs199643713
NM_001109878.2(TBX22):c.799-13A>G
NM_001109878.2(TBX22):c.804G>A (p.Thr268=) rs150811689
NM_001109878.2(TBX22):c.864-11C>T
NM_001109878.2(TBX22):c.883T>C (p.Leu295=) rs195293
NM_001109878.2(TBX22):c.949+12T>G rs151121450

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