ClinVar Miner

List of variants reported as likely pathogenic for polydactyly-syndactyly-triphalangism by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

Included ClinVar conditions (78):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_001077418.3(TMEM231):c.664G>A (p.Val222Ile) rs397514753 0.00005
NM_001329943.3(KIAA0586):c.2407T>G (p.Ser803Ala) rs886039806 0.00003
NC_000019.10:g.45227673dup rs886039793
NM_001044385.3(TMEM237):c.869+1G>A rs730882231
NM_001164405.2(BHLHA9):c.218G>T (p.Arg73Leu)
NM_001173990.3(TMEM216):c.218G>A (p.Arg73His) rs201108965
NM_001378615.1(CC2D2A):c.2339-2A>C rs1719092280
NM_001378615.1(CC2D2A):c.4531T>C (p.Trp1511Arg) rs1721483506
NM_001382391.1(CSPP1):c.2259_2262del (p.Glu755fs) rs587777145
NM_016464.5(TMEM138):c.134A>G (p.Gln45Arg) rs886039804
NM_021807.4(EXOC4):c.1733A>G (p.Gln578Arg) rs730882233
NM_024715.4(TXNDC15):c.103+1G>A rs886039792
NM_024715.4(TXNDC15):c.673_687del (p.Ser225_His229del) rs886039791
NM_147127.5(EVC2):c.3870_3893dup (p.Lys1293_Lys1300dup) rs730882232
NM_152515.5(CKAP2L):c.1604G>A (p.Gly535Asp)
NM_198525.3(KIF7):c.2286_2287insT (p.Gln763fs) rs1963937785

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