"Invitae"[submitter] AND "KIRREL3"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 731455	NM_032531.4(KIRREL3):c.2280G>A (p.Ser760=)	KIRREL3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 129426	NM_032531.4(KIRREL3):c.2151C>T (p.Ser717=)	KIRREL3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 725838	NM_032531.4(KIRREL3):c.2118T>G (p.Leu706=)	KIRREL3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 211304	NM_032531.4(KIRREL3):c.1983G>A (p.Leu661=)	KIRREL3	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 790850	NM_032531.4(KIRREL3):c.1791C>T (p.Thr597=)	KIRREL3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 761861	NM_032531.4(KIRREL3):c.1470G>A (p.Arg490=)	KIRREL3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 211302	NM_032531.4(KIRREL3):c.1395G>A (p.Ser465=)	KIRREL3	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 731655	NM_032531.4(KIRREL3):c.1386G>A (p.Ser462=)	KIRREL3	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 379453	NM_032531.4(KIRREL3):c.1166G>A (p.Arg389His)	KIRREL3 (R389H)	Single nucleotide variant (missense variant)	not specified +1 more	GLikely benign
Select item 744281	NM_032531.4(KIRREL3):c.1098C>T (p.Ile366=)	KIRREL3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 735371	NM_032531.4(KIRREL3):c.998-4G>A	KIRREL3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 746186	NM_032531.4(KIRREL3):c.885T>C (p.Ser295=)	KIRREL3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 725236	NM_032531.4(KIRREL3):c.756C>T (p.Val252=)	KIRREL3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 211307	NM_032531.4(KIRREL3):c.396C>T (p.Ala132=)	KIRREL3	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 791497	NM_032531.4(KIRREL3):c.249C>T (p.Asp83=)	KIRREL3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 707953	NM_032531.4(KIRREL3):c.222C>T (p.Tyr74=)	KIRREL3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign