List of variants in gene HNRNPDL reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_031372.4(HNRNPDL):c.125T>C (p.Leu42Pro)	rs61729823	0.00443
NM_031372.4(HNRNPDL):c.124C>T (p.Leu42Phe)	rs200018272	0.00441
NM_031372.4(HNRNPDL):c.330G>A (p.Gln110=)	rs370279130	0.00072
NM_031372.4(HNRNPDL):c.21T>C (p.Leu7=)	rs778302994	0.00004
NM_031372.4(HNRNPDL):c.61A>G (p.Thr21Ala)	rs1057389514	0.00001
NM_031372.4(HNRNPDL):c.1108A>C (p.Asn370His)	rs1057519137
NM_031372.4(HNRNPDL):c.115_116delinsTT (p.Ala39Phe)	rs2110031828
NM_031372.4(HNRNPDL):c.136G>C (p.Ala46Pro)
NM_031372.4(HNRNPDL):c.153G>A (p.Arg51=)	rs370944367
NM_031372.4(HNRNPDL):c.262C>T (p.Arg88Cys)
NM_031372.4(HNRNPDL):c.316C>T (p.Arg106Trp)	rs140163739
NM_031372.4(HNRNPDL):c.325C>T (p.Arg109Cys)
NM_031372.4(HNRNPDL):c.552C>A (p.Val184=)
NM_031372.4(HNRNPDL):c.99_113del (p.Pro34_Leu38del)	rs1057519138

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