Related gene-specific medical variations for Gene (Select 120237) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3080225	NM_001029865.4(DBX1):c.973T>C (p.Phe325Leu)	DBX1, LOC126861159 (F325L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080224	NM_001029865.4(DBX1):c.940G>A (p.Ala314Thr)	DBX1, LOC126861159 (A314T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080223	NM_001029865.4(DBX1):c.931C>A (p.Pro311Thr)	DBX1, LOC126861159 (P311T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3080222	NM_001029865.4(DBX1):c.511C>A (p.Pro171Thr)	DBX1, LOC126861159 (P171T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641685	NM_001029865.4(DBX1):c.735G>A (p.Leu245=)	LOC126861159, DBX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2604311	NM_001029865.4(DBX1):c.766C>T (p.Pro256Ser)	DBX1, LOC126861159 (P256S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542140	NM_001029865.4(DBX1):c.737C>G (p.Ser246Cys)	DBX1, LOC126861159 (S246C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462604	NM_001029865.4(DBX1):c.827A>C (p.Glu276Ala)	DBX1, LOC126861159 (E276A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371149	NM_001029865.4(DBX1):c.812A>G (p.Lys271Arg)	DBX1, LOC126861159 (K271R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293993	NM_001029865.4(DBX1):c.919G>C (p.Gly307Arg)	DBX1, LOC126861159 (G307R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275123	NM_001029865.4(DBX1):c.734T>G (p.Leu245Arg)	DBX1, LOC126861159 (L245R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206329	NM_001029865.4(DBX1):c.818C>A (p.Pro273His)	DBX1, LOC126861159 (P273H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance