Related gene-specific medical variations for Gene (Select 389337) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3313813	NM_001001669.3(ARHGEF37):c.1957G>C (p.Gly653Arg)	ARHGEF37, LOC126807550 (G653R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313802	NM_001001669.3(ARHGEF37):c.722A>G (p.His241Arg)	ARHGEF37, LOC129994963 (H241R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129302	NM_001001669.3(ARHGEF37):c.745C>T (p.Arg249Trp)	ARHGEF37, LOC129994963 (R249W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3129301	NM_001001669.3(ARHGEF37):c.669C>T (p.Tyr223=)	ARHGEF37, LOC129994963	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2655899	NM_001001669.3(ARHGEF37):c.1830G>A (p.Ala610=)	ARHGEF37, LOC126807550	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2598564	NM_001001669.3(ARHGEF37):c.676G>A (p.Val226Ile)	ARHGEF37, LOC129994963 (V226I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510840	NM_001001669.3(ARHGEF37):c.779T>G (p.Leu260Arg)	ARHGEF37, LOC129994963 (L260R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400315	NM_001001669.3(ARHGEF37):c.1829C>T (p.Ala610Val)	ARHGEF37, LOC126807550 (A610V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2238020	NM_001001669.3(ARHGEF37):c.1841T>C (p.Val614Ala)	ARHGEF37, LOC126807550 (V614A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance