Related gene-specific medical variations for Gene (Select 9278) - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3333887	NM_005453.5(ZBTB22):c.1226C>G (p.Pro409Arg)	LOC123620086, ZBTB22 (P409R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191958	NM_005453.5(ZBTB22):c.1427G>A (p.Gly476Glu)	LOC123620086, ZBTB22 (G476E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191957	NM_005453.5(ZBTB22):c.1389C>G (p.Ser463Arg)	LOC123620086, ZBTB22 (S463R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191956	NM_005453.5(ZBTB22):c.1287C>G (p.Phe429Leu)	LOC123620086, ZBTB22 (F429L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191955	NM_005453.5(ZBTB22):c.1172G>T (p.Gly391Val)	LOC123620086, ZBTB22 (G391V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191954	NM_005453.5(ZBTB22):c.1162G>A (p.Glu388Lys)	LOC123620086, ZBTB22 (E388K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588049	NM_005453.5(ZBTB22):c.1222G>C (p.Ala408Pro)	LOC123620086, ZBTB22 (A408P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548824	NM_005453.5(ZBTB22):c.1018C>G (p.Leu340Val)	LOC123620086, ZBTB22 (L340V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548073	NM_005453.5(ZBTB22):c.1070G>A (p.Ser357Asn)	LOC123620086, ZBTB22 (S357N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496161	NM_005453.5(ZBTB22):c.1336G>A (p.Gly446Arg)	LOC123620086, ZBTB22 (G446R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482243	NM_005453.5(ZBTB22):c.1399C>T (p.Pro467Ser)	LOC123620086, ZBTB22 (P467S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343136	NM_005453.5(ZBTB22):c.1243C>T (p.Pro415Ser)	LOC123620086, ZBTB22 (P415S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234493	NM_005453.5(ZBTB22):c.1394G>A (p.Gly465Asp)	LOC123620086, ZBTB22 (G465D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance