HP1BP3[gene] and "single gene"[properties] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2492053	NM_001372052.1(HP1BP3):c.1624A>C (p.Lys542Gln)	HP1BP3 (K542Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 711751	NM_001372052.1(HP1BP3):c.1593A>G (p.Ala531=)	HP1BP3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3106773	NM_001372052.1(HP1BP3):c.1523A>C (p.Lys508Thr)	HP1BP3 (K470T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216773	NM_001372052.1(HP1BP3):c.1408G>A (p.Ala470Thr)	HP1BP3 (A469T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2274966	NM_001372052.1(HP1BP3):c.1403A>G (p.Lys468Arg)	HP1BP3 (K467R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2255765	NM_001372052.1(HP1BP3):c.1397C>T (p.Pro466Leu)	HP1BP3 (P428L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607162	NM_001372052.1(HP1BP3):c.1331A>G (p.Glu444Gly)	HP1BP3 (E406G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106772	NM_001372052.1(HP1BP3):c.1294A>G (p.Arg432Gly)	HP1BP3 (R432G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106771	NM_001372052.1(HP1BP3):c.1278A>C (p.Lys426Asn)	HP1BP3 (K425N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106770	NM_001372052.1(HP1BP3):c.1277A>G (p.Lys426Arg)	HP1BP3 (K425R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328989	NM_001372052.1(HP1BP3):c.1024A>C (p.Met342Leu)	HP1BP3 (M342L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106769	NM_001372052.1(HP1BP3):c.1009C>T (p.Leu337Phe)	HP1BP3 (L299F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339311	NM_001372052.1(HP1BP3):c.1004C>T (p.Pro335Leu)	HP1BP3 (P334L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239283	NM_001372052.1(HP1BP3):c.937C>G (p.Gln313Glu)	HP1BP3 (Q313E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301119	NM_001372052.1(HP1BP3):c.910G>A (p.Ala304Thr)	HP1BP3 (A304T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106776	NM_001372052.1(HP1BP3):c.334G>A (p.Glu112Lys)	HP1BP3 (E74K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3284710	NM_001372052.1(HP1BP3):c.311A>G (p.Glu104Gly)	HP1BP3 (E66G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2283754	NM_001372052.1(HP1BP3):c.265A>G (p.Thr89Ala)	HP1BP3 (T89A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2388126	NM_001372052.1(HP1BP3):c.262G>C (p.Ala88Pro)	HP1BP3 (A88P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522849	NM_001372052.1(HP1BP3):c.113C>T (p.Thr38Ile)	HP1BP3 (T37I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2466982	NM_001372052.1(HP1BP3):c.79G>A (p.Ala27Thr)	HP1BP3 (A27T)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2479582	NM_001372052.1(HP1BP3):c.56T>C (p.Ile19Thr)	HP1BP3 (I19T)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3106774	NM_001372052.1(HP1BP3):c.16T>G (p.Ser6Ala)	HP1BP3 (S6A)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance

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Items: 23