"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "DHX37"[gen - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 735695	NM_032656.4(DHX37):c.3440T>C (p.Ile1147Thr)	DHX37 (I1147T)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3025788	NM_032656.4(DHX37):c.3301C>T (p.Arg1101Cys)	DHX37 (R1101C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2182100	NM_032656.4(DHX37):c.3216+3A>G	DHX37	Single nucleotide variant (intron variant)	not provided	GConflicting classifications of pathogenicity
Select item 2255128	NM_032656.4(DHX37):c.3178C>T (p.Arg1060Cys)	DHX37 (R1060C)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 1675520	NM_032656.4(DHX37):c.3092G>A (p.Arg1031Gln)	DHX37 (R1031Q)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 2161758	NM_032656.4(DHX37):c.3082G>A (p.Glu1028Lys)	DHX37 (E1028K)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2168184	NM_032656.4(DHX37):c.3078C>T (p.Cys1026=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2643577	NM_032656.4(DHX37):c.2691C>T (p.Thr897=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2643578	NM_032656.4(DHX37):c.2504G>A (p.Arg835Gln)	DHX37 (R835Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2054636	NM_032656.4(DHX37):c.2288G>A (p.Arg763Gln)	DHX37 (R763Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1176972	NM_032656.4(DHX37):c.2227G>A (p.Ala743Thr)	DHX37 (A743T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2672532	NM_032656.4(DHX37):c.2211C>T (p.Ala737=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2643579	NM_032656.4(DHX37):c.2061G>A (p.Ala687=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2054907	NM_032656.4(DHX37):c.1953C>T (p.Gly651=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2344260	NM_032656.4(DHX37):c.1681G>A (p.Gly561Arg)	DHX37 (G561R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1879247	NM_032656.4(DHX37):c.1638C>T (p.Gly546=)	DHX37	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 691925	NM_032656.4(DHX37):c.1399C>G (p.Leu467Val)	DHX37 (L467V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2643580	NM_032656.4(DHX37):c.1105G>A (p.Val369Met)	DHX37 (V369M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2643581	NM_032656.4(DHX37):c.932C>T (p.Ala311Val)	DHX37 (A311V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2150650	NM_032656.4(DHX37):c.816C>T (p.Ile272=)	DHX37	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2643582	NM_032656.4(DHX37):c.729G>A (p.Pro243=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2643583	NM_032656.4(DHX37):c.703G>A (p.Val235Ile)	DHX37 (V235I)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2014567	NM_032656.4(DHX37):c.478GAG[10] (p.Glu168_Ser169insGlu)	DHX37	Microsatellite (inframe_insertion)	not provided +1 more	GBenign/Likely benign
Select item 2672533	NM_032656.4(DHX37):c.405G>A (p.Val135=)	DHX37	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3067308	NM_032656.4(DHX37):c.399C>G (p.Asp133Glu)	DHX37 (D133E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1694691	NM_032656.4(DHX37):c.369C>A (p.Asn123Lys)	DHX37 (N123K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 716809	NM_032656.4(DHX37):c.182C>T (p.Ala61Val)	DHX37 (A61V)	Single nucleotide variant (missense variant)	DHX37-related condition +1 more	GBenign/Likely benign
Select item 716810	NM_032656.4(DHX37):c.42G>A (p.Gln14=)	DHX37, LOC130009166	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 28