Related gene-specific medical variations for Gene (Select 54851) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3126854	NM_017704.3(ANKRD49):c.460A>G (p.Thr154Ala)	ANKRD49, MRE11 (T154A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126853	NM_017704.3(ANKRD49):c.255T>A (p.Asn85Lys)	ANKRD49, MRE11 (N85K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380501	NM_017704.3(ANKRD49):c.136G>A (p.Val46Ile)	ANKRD49, MRE11 (V46I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310121	NM_017704.3(ANKRD49):c.291G>C (p.Lys97Asn)	ANKRD49, MRE11 (K97N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298995	NM_017704.3(ANKRD49):c.20A>G (p.Asn7Ser)	ANKRD49, MRE11 (N7S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1203262	NM_017704.3(ANKRD49):c.-91+7T>C	ANKRD49, MRE11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 403103	NM_017704.3(ANKRD49):c.279C>G (p.Leu93=)	ANKRD49, MRE11	Single nucleotide variant (synonymous variant)	not specified	GBenign

ClinVar