C5231481[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar - NCBI

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Search results

Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1255483	NM_032656.4(DHX37):c.3242G>A (p.Arg1081Gln)	DHX37 (R1081Q)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 1255484	NM_032656.4(DHX37):c.3195C>T (p.Ala1065=)	DHX37	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1255485	NM_032656.4(DHX37):c.2869-38G>A	DHX37	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1251560	NM_032656.4(DHX37):c.2793A>G (p.Ala931=)	DHX37	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1255486	NM_032656.4(DHX37):c.2696-26G>A	DHX37	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1255487	NM_032656.4(DHX37):c.2695+12T>C	DHX37	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1255488	NM_032656.4(DHX37):c.2605A>G (p.Ser869Gly)	DHX37 (S869G)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 1255489	NM_032656.4(DHX37):c.2598G>A (p.Glu866=)	DHX37	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 1255490	NM_032656.4(DHX37):c.2579-7T>C	DHX37	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1255491	NM_032656.4(DHX37):c.2578+17T>G	DHX37	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1255492	NM_032656.4(DHX37):c.2331A>G (p.Thr777=)	DHX37	Single nucleotide variant (synonymous variant)	46,XY sex reversal 11 +2 more	GBenign
Select item 1255493	NM_032656.4(DHX37):c.2046-6A>G	DHX37	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1255494	NM_032656.4(DHX37):c.1294-38T>C	DHX37	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1255495	NM_032656.4(DHX37):c.738+13G>A	DHX37	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 1255496	NM_032656.4(DHX37):c.288G>A (p.Met96Ile)	DHX37 (M96I)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign