Related gene-specific medical variations for Gene (Select 116985) - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3309406	NM_001040118.3(ARAP1):c.2096C>T (p.Thr699Met)	ARAP1, ARAP1-AS2 (T699M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128199	NM_001040118.3(ARAP1):c.2158C>G (p.Arg720Gly)	ARAP1, ARAP1-AS2 (R475G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3128197	NM_001040118.3(ARAP1):c.1952G>A (p.Arg651His)	ARAP1, ARAP1-AS2 (R406H +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3128196	NM_001040118.3(ARAP1):c.1949G>A (p.Arg650His)	ARAP1, ARAP1-AS2 (R405H +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3128195	NM_001040118.3(ARAP1):c.1904C>G (p.Thr635Ser)	ARAP1, ARAP1-AS2 (T635S +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3128194	NM_001040118.3(ARAP1):c.1855G>C (p.Ala619Pro)	ARAP1, ARAP1-AS2 (A374P +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2380563	NM_001040118.3(ARAP1):c.2104G>A (p.Ala702Thr)	ARAP1, ARAP1-AS2 (A396T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2371531	NM_001040118.3(ARAP1):c.2158C>T (p.Arg720Trp)	ARAP1, ARAP1-AS2 (R414W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352011	NM_001040118.3(ARAP1):c.1843C>T (p.Arg615Cys)	ARAP1, ARAP1-AS2 (R615C +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2351868	NM_001040118.3(ARAP1):c.1865C>T (p.Pro622Leu)	ARAP1, ARAP1-AS2 (P377L +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2274175	NM_001040118.3(ARAP1):c.1834G>A (p.Ala612Thr)	ARAP1, ARAP1-AS2 (A367T +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2264709	NM_001040118.3(ARAP1):c.2288G>A (p.Arg763His)	ARAP1, ARAP1-AS2 (R457H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242346	NM_001040118.3(ARAP1):c.2194C>A (p.Pro732Thr)	ARAP1, ARAP1-AS2 (P732T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220039	NM_001040118.3(ARAP1):c.2039C>T (p.Ala680Val)	ARAP1, ARAP1-AS2 (A374V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 786599	NM_001040118.3(ARAP1):c.2168-10G>A	ARAP1, ARAP1-AS2	Single nucleotide variant (intron variant)	not provided	GBenign