Related gene-specific medical variations for Gene (Select 643664) - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3319662	NM_001102614.2(SLC35G6):c.712C>G (p.Leu238Val)	SLC35G6, ZBTB4 (L238V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3319661	NM_001102614.2(SLC35G6):c.818C>T (p.Ala273Val)	SLC35G6, ZBTB4 (A273V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3319660	NM_001102614.2(SLC35G6):c.248T>C (p.Ile83Thr)	SLC35G6, ZBTB4 (I83T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3319659	NM_001102614.2(SLC35G6):c.554C>T (p.Thr185Met)	SLC35G6, ZBTB4 (T185M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3164473	NM_001102614.2(SLC35G6):c.547G>A (p.Gly183Arg)	SLC35G6, ZBTB4 (G183R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3164472	NM_001102614.2(SLC35G6):c.418G>A (p.Val140Ile)	SLC35G6, ZBTB4 (V140I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3164471	NM_001102614.2(SLC35G6):c.334G>A (p.Val112Ile)	SLC35G6, ZBTB4 (V112I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3164470	NM_001102614.2(SLC35G6):c.268C>T (p.Arg90Cys)	SLC35G6, ZBTB4 (R90C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2681554	NM_001102614.2(SLC35G6):c.269G>A (p.Arg90His)	SLC35G6, ZBTB4 (R90H)	Single nucleotide variant (missense variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2681553	NM_001102614.2(SLC35G6):c.176A>G (p.His59Arg)	SLC35G6, ZBTB4 (H59R)	Single nucleotide variant (missense variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2607856	NM_001102614.2(SLC35G6):c.61G>A (p.Ala21Thr)	SLC35G6, ZBTB4 (A21T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2592008	NM_001102614.2(SLC35G6):c.592G>T (p.Val198Leu)	SLC35G6, ZBTB4 (V198L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2551449	NM_001102614.2(SLC35G6):c.496A>T (p.Ile166Phe)	SLC35G6, ZBTB4 (I166F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2549540	NM_001102614.2(SLC35G6):c.1010A>G (p.Glu337Gly)	SLC35G6, ZBTB4 (E337G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546823	NM_001102614.2(SLC35G6):c.727C>T (p.Pro243Ser)	SLC35G6, ZBTB4 (P243S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546812	NM_001102614.2(SLC35G6):c.301C>G (p.Arg101Gly)	SLC35G6, ZBTB4 (R101G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546803	NM_001102614.2(SLC35G6):c.276C>A (p.Asp92Glu)	SLC35G6, ZBTB4 (D92E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533412	NM_001102614.2(SLC35G6):c.878C>T (p.Ala293Val)	SLC35G6, ZBTB4 (A293V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529320	NM_001102614.2(SLC35G6):c.974C>G (p.Ala325Gly)	SLC35G6, ZBTB4 (A325G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511376	NM_001102614.2(SLC35G6):c.605C>T (p.Ala202Val)	SLC35G6, ZBTB4 (A202V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507970	NM_001102614.2(SLC35G6):c.401G>C (p.Arg134Pro)	SLC35G6, ZBTB4 (R134P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454724	NM_001102614.2(SLC35G6):c.566C>A (p.Thr189Asn)	SLC35G6, ZBTB4 (T189N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398065	NM_001102614.2(SLC35G6):c.352G>A (p.Ala118Thr)	SLC35G6, ZBTB4 (A118T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389376	NM_001102614.2(SLC35G6):c.124G>C (p.Val42Leu)	SLC35G6, ZBTB4 (V42L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376575	NM_001102614.2(SLC35G6):c.475T>G (p.Trp159Gly)	SLC35G6, ZBTB4 (W159G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352220	NM_001102614.2(SLC35G6):c.50C>T (p.Ser17Leu)	SLC35G6, ZBTB4 (S17L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299800	NM_001102614.2(SLC35G6):c.950T>C (p.Leu317Pro)	SLC35G6, ZBTB4 (L317P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2274418	NM_001102614.2(SLC35G6):c.332A>C (p.Asn111Thr)	SLC35G6, ZBTB4 (N111T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267495	NM_001102614.2(SLC35G6):c.643T>C (p.Phe215Leu)	SLC35G6, ZBTB4 (F215L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2265511	NM_001102614.2(SLC35G6):c.734T>C (p.Val245Ala)	SLC35G6, ZBTB4 (V245A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256673	NM_001102614.2(SLC35G6):c.419T>G (p.Val140Gly)	SLC35G6, ZBTB4 (V140G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213955	NM_001102614.2(SLC35G6):c.517G>A (p.Val173Met)	SLC35G6, ZBTB4 (V173M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Links from Gene

Items: 32