"Ambry Genetics"[submitter] AND "LOC126861124"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3139700	NM_176875.4(CCKBR):c.535T>G (p.Trp179Gly)	CCKBR, LOC126861124 (W179G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139701	NM_176875.4(CCKBR):c.602G>A (p.Arg201His)	CCKBR, LOC126861124 (R117H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257649	NM_176875.4(CCKBR):c.662T>C (p.Leu221Pro)	CCKBR, LOC126861124 (L137P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139702	NM_176875.4(CCKBR):c.809C>T (p.Pro270Leu)	CCKBR, LOC126861124 (P186L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139703	NM_176875.4(CCKBR):c.830G>C (p.Gly277Ala)	CCKBR, LOC126861124 (G193A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292640	NM_176875.4(CCKBR):c.832C>A (p.Arg278Ser)	CCKBR, LOC126861124 (R347S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495650	NM_176875.4(CCKBR):c.870C>A (p.Ser290Arg)	CCKBR, LOC126861124 (S206R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615085	NM_176875.4(CCKBR):c.877T>C (p.Cys293Arg)	CCKBR, LOC126861124 (C209R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139704	NM_176875.4(CCKBR):c.887A>C (p.Gln296Pro)	CCKBR, LOC126861124 (Q212P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139705	NM_176875.4(CCKBR):c.902G>T (p.Arg301Leu)	CCKBR, LOC126861124 (R217L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510264	NM_176875.4(CCKBR):c.958C>T (p.Pro320Ser)	CCKBR, LOC126861124 (P320S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance