Related gene-specific medical variations for Gene (Select 158586) - ClinVar

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Links from Gene

Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3260201	NM_007157.4(ZXDB):c.796C>T (p.Pro266Ser)	LOC130068357, ZXDB (P266S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260195	NM_007157.4(ZXDB):c.541G>C (p.Glu181Gln)	LOC130068356, ZXDB (E181Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199674	NM_007157.4(ZXDB):c.782C>T (p.Pro261Leu)	LOC130068357, ZXDB (P261L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199673	NM_007157.4(ZXDB):c.755C>T (p.Pro252Leu)	LOC130068357, ZXDB (P252L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199672	NM_007157.4(ZXDB):c.662C>T (p.Pro221Leu)	LOC130068357, ZXDB (P221L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199670	NM_007157.4(ZXDB):c.590C>T (p.Pro197Leu)	LOC130068356, ZXDB (P197L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199669	NM_007157.4(ZXDB):c.540T>G (p.Phe180Leu)	LOC130068356, ZXDB (F180L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2660729	NM_007157.4(ZXDB):c.795C>T (p.Gly265=)	LOC130068357, ZXDB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660728	NM_007157.4(ZXDB):c.792C>T (p.Ser264=)	LOC130068357, ZXDB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2660727	NM_007157.4(ZXDB):c.498G>A (p.Ala166=)	LOC130068356, ZXDB	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2603837	NM_007157.4(ZXDB):c.836G>C (p.Gly279Ala)	LOC130068357, ZXDB (G279A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549193	NM_007157.4(ZXDB):c.337G>A (p.Ala113Thr)	LOC130068356, ZXDB (A113T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2549192	NM_007157.4(ZXDB):c.328G>A (p.Gly110Ser)	LOC130068356, ZXDB (G110S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542490	NM_007157.4(ZXDB):c.683C>G (p.Pro228Arg)	LOC130068357, ZXDB (P228R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526962	NM_007157.4(ZXDB):c.725C>T (p.Ala242Val)	LOC130068357, ZXDB (A242V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405810	NM_007157.4(ZXDB):c.418A>T (p.Thr140Ser)	LOC130068356, ZXDB (T140S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401239	NM_007157.4(ZXDB):c.401C>T (p.Ala134Val)	LOC130068356, ZXDB (A134V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398585	NM_007157.4(ZXDB):c.351G>T (p.Leu117Phe)	LOC130068356, ZXDB (L117F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385115	NM_007157.4(ZXDB):c.425T>A (p.Leu142Gln)	LOC130068356, ZXDB (L142Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367043	NM_007157.4(ZXDB):c.580G>C (p.Ala194Pro)	LOC130068356, ZXDB (A194P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361472	NM_007157.4(ZXDB):c.547G>C (p.Gly183Arg)	LOC130068356, ZXDB (G183R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357198	NM_007157.4(ZXDB):c.434G>A (p.Arg145His)	LOC130068356, ZXDB (R145H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354089	NM_007157.4(ZXDB):c.659A>C (p.His220Pro)	LOC130068357, ZXDB (H220P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346988	NM_007157.4(ZXDB):c.799G>T (p.Gly267Cys)	LOC130068357, ZXDB (G267C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315809	NM_007157.4(ZXDB):c.665G>A (p.Gly222Asp)	LOC130068357, ZXDB (G222D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310907	NM_007157.4(ZXDB):c.323G>C (p.Gly108Ala)	LOC130068356, ZXDB (G108A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292982	NM_007157.4(ZXDB):c.371G>T (p.Gly124Val)	LOC130068356, ZXDB (G124V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 27