"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1320 - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2918130	NM_001447.3(FAT2):c.10593T>C (p.Ala3531=)	FAT2, LOC132089193 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1251356	NM_001447.3(FAT2):c.10557C>G (p.Val3519=)	FAT2, LOC132089193 +1 more	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 717651	NM_001447.3(FAT2):c.10553G>A (p.Arg3518His)	FAT2, LOC132089193 +1 more (R3518H)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 2959675	NM_001447.3(FAT2):c.10552C>T (p.Arg3518Cys)	FAT2, LOC132089193 +1 more (R3518C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2970235	NM_001447.3(FAT2):c.10545G>A (p.Thr3515=)	FAT2, LOC132089193 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2173071	NM_001447.3(FAT2):c.10544C>T (p.Thr3515Met)	FAT2, LOC132089193 +1 more (T3515M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1232448	NM_001447.3(FAT2):c.10541T>C (p.Leu3514Ser)	FAT2, LOC132089193 +1 more (L3514S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1265696	NM_001447.3(FAT2):c.10524C>A (p.Ile3508=)	FAT2, LOC132089193 +1 more	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 730896	NM_001447.3(FAT2):c.10509G>A (p.Ala3503=)	LOC132089193, SLC36A1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3003808	NM_001447.3(FAT2):c.10508C>T (p.Ala3503Val)	FAT2, LOC132089193 +1 more (A3503V)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity