Related gene-specific medical variations for Gene (Select 2769) - ClinVar - NCBI

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Links from Gene

Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3100557	NM_002068.4(GNA15):c.504G>T (p.Glu168Asp)	GNA15, GNA15-DT (E168D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100556	NM_002068.4(GNA15):c.215A>T (p.Glu72Val)	GNA15, GNA15-DT (E72V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3100555	NM_002068.4(GNA15):c.212C>T (p.Ser71Leu)	GNA15, GNA15-DT (S71L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3100554	NM_002068.4(GNA15):c.205G>A (p.Gly69Ser)	GNA15, GNA15-DT (G69S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2603084	NM_002068.4(GNA15):c.550C>T (p.Arg184Cys)	GNA15, GNA15-DT (R184C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592785	NM_002068.4(GNA15):c.976G>T (p.Gly326Cys)	GNA15, LOC112543480 (G326C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2537446	NM_002068.4(GNA15):c.496C>T (p.His166Tyr)	GNA15, GNA15-DT (H166Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530056	NM_002068.4(GNA15):c.604A>G (p.Thr202Ala)	GNA15, GNA15-DT (T202A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495240	NM_002068.4(GNA15):c.467T>A (p.Leu156Gln)	GNA15, GNA15-DT (L156Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492601	NM_002068.4(GNA15):c.278T>C (p.Met93Thr)	GNA15, GNA15-DT (M93T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2379424	NM_002068.4(GNA15):c.595G>A (p.Val199Met)	GNA15, GNA15-DT (V199M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365704	NM_002068.4(GNA15):c.544G>A (p.Val182Met)	GNA15, GNA15-DT (V182M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355656	NM_002068.4(GNA15):c.202G>A (p.Ala68Thr)	GNA15, GNA15-DT (A68T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2252777	NM_002068.4(GNA15):c.505C>T (p.Arg169Cys)	GNA15, GNA15-DT (R169C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 790433	NM_002068.4(GNA15):c.561G>A (p.Met187Ile)	GNA15, GNA15-DT (M187I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 786961	NM_002068.4(GNA15):c.341G>A (p.Ser114Asn)	GNA15-DT, GNA15 (S114N)	Single nucleotide variant (missense variant)	not provided	GBenign