"Ambry Genetics"[submitter] AND "LOC643327"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2407203	NM_015482.2(SLC22A23):c.650G>A (p.Ser217Asn)	LOC643327, SLC22A23 (S217N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3163431	NM_015482.2(SLC22A23):c.616G>C (p.Gly206Arg)	LOC643327, SLC22A23 (G206R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508276	NM_015482.2(SLC22A23):c.590A>G (p.Asn197Ser)	LOC643327, SLC22A23 (N197S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2309189	NM_015482.2(SLC22A23):c.448G>C (p.Gly150Arg)	LOC643327, SLC22A23 (G150R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402418	NM_015482.2(SLC22A23):c.447G>T (p.Met149Ile)	LOC643327, SLC22A23 (M149I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473049	NM_015482.2(SLC22A23):c.392C>T (p.Ala131Val)	LOC643327, SLC22A23 (A131V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456798	NM_015482.2(SLC22A23):c.262C>T (p.Leu88Phe)	LOC643327, SLC22A23 (L88F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220673	NM_015482.2(SLC22A23):c.128G>A (p.Gly43Asp)	LOC643327, SLC22A23 (G43D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619611	NM_015482.2(SLC22A23):c.118G>A (p.Gly40Arg)	LOC643327, SLC22A23 (G40R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238164	NM_015482.2(SLC22A23):c.107C>G (p.Ala36Gly)	LOC643327, SLC22A23 (A36G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615708	NM_015482.2(SLC22A23):c.40C>T (p.Pro14Ser)	LOC643327, SLC22A23 (P14S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250894	NM_015482.2(SLC22A23):c.14G>A (p.Arg5Gln)	LOC643327, SLC22A23 (R5Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349542	NM_015482.2(SLC22A23):c.7A>G (p.Ile3Val)	LOC643327, SLC22A23 (I3V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance