Related gene-specific medical variations for Gene (Select 84709) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3294594	NM_032623.4(MGARP):c.710C>T (p.Ser237Leu)	LOC126807166, MGARP (S237L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3294593	NM_032623.4(MGARP):c.361G>A (p.Asp121Asn)	LOC126807166, MGARP (D121N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125894	NM_032623.4(MGARP):c.566C>T (p.Thr189Ile)	LOC126807166, MGARP (T189I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125893	NM_032623.4(MGARP):c.289G>A (p.Glu97Lys)	LOC126807166, MGARP (E97K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611367	NM_032623.4(MGARP):c.527C>T (p.Thr176Ile)	LOC126807166, MGARP (T176I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591196	NM_032623.4(MGARP):c.56C>T (p.Pro19Leu)	LOC129993105, MGARP (P19L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392222	NM_032623.4(MGARP):c.529C>T (p.Pro177Ser)	LOC126807166, MGARP (P177S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2325171	NM_032623.4(MGARP):c.400A>G (p.Lys134Glu)	LOC126807166, MGARP (K134E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2317638	NM_032623.4(MGARP):c.313G>T (p.Ala105Ser)	LOC126807166, MGARP (A105S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259295	NM_032623.4(MGARP):c.532G>A (p.Glu178Lys)	LOC126807166, MGARP (E178K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance