SPOCD1[gene] and "single gene"[properties] - ClinVar

Search results

Items: 85

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3169267	NM_144569.7(SPOCD1):c.3646G>T (p.Ala1216Ser)	SPOCD1 (A1216S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2272545	NM_144569.7(SPOCD1):c.3587G>A (p.Arg1196His)	SPOCD1 (R1196H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397061	NM_144569.7(SPOCD1):c.3586C>T (p.Arg1196Cys)	SPOCD1 (R447C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354459	NM_144569.7(SPOCD1):c.3542G>A (p.Arg1181His)	SPOCD1 (R661H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2231254	NM_144569.7(SPOCD1):c.3505C>T (p.Pro1169Ser)	SPOCD1 (P1156S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223613	NM_144569.7(SPOCD1):c.3460G>A (p.Glu1154Lys)	SPOCD1 (E1141K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3322313	NM_144569.7(SPOCD1):c.3451C>G (p.Arg1151Gly)	SPOCD1 (R444G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2593683	NM_144569.7(SPOCD1):c.3451C>T (p.Arg1151Trp)	SPOCD1 (R1138W +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454643	NM_144569.7(SPOCD1):c.3422G>A (p.Arg1141Lys)	SPOCD1 (R1128K +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3322314	NM_144569.7(SPOCD1):c.3383C>A (p.Pro1128Gln)	SPOCD1 (P1128Q +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2626779	NM_144569.7(SPOCD1):c.3354_3355insA (p.Gln1119fs)	SPOCD1 (Q1106fs +4 more)	Insertion (frameshift variant +1 more)	Male infertility with azoospermia or oligozoospermia due to single gene mutation	GLikely pathogenic
Select item 2588422	NM_144569.7(SPOCD1):c.3353G>A (p.Arg1118His)	SPOCD1 (R598H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2514756	NM_144569.7(SPOCD1):c.3352C>T (p.Arg1118Cys)	SPOCD1 (R369C +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3169266	NM_144569.7(SPOCD1):c.3334C>T (p.Pro1112Ser)	SPOCD1 (P1112S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457763	NM_144569.7(SPOCD1):c.3325G>A (p.Gly1109Arg)	SPOCD1 (G1109R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379009	NM_144569.7(SPOCD1):c.3238C>T (p.Pro1080Ser)	SPOCD1 (P1067S +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543945	NM_144569.7(SPOCD1):c.3205T>G (p.Trp1069Gly)	SPOCD1 (W1056G +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2595224	NM_144569.7(SPOCD1):c.3191C>T (p.Pro1064Leu)	SPOCD1 (P1064L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483941	NM_144569.7(SPOCD1):c.3188C>T (p.Pro1063Leu)	SPOCD1 (P314L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2555030	NM_144569.7(SPOCD1):c.2971G>A (p.Ala991Thr)	SPOCD1 (A991T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3322315	NM_144569.7(SPOCD1):c.2918C>T (p.Ala973Val)	SPOCD1 (A279V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2626778	NM_144569.7(SPOCD1):c.2912T>G (p.Leu971Arg)	SPOCD1 (L464R +3 more)	Single nucleotide variant (missense variant +1 more)	Male infertility with azoospermia or oligozoospermia due to single gene mutation	GLikely pathogenic
Select item 3322316	NM_144569.7(SPOCD1):c.2864G>A (p.Arg955His)	SPOCD1 (R219H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342505	NM_144569.7(SPOCD1):c.2852A>G (p.Asn951Ser)	SPOCD1 (N951S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2243760	NM_144569.7(SPOCD1):c.2800C>T (p.Pro934Ser)	SPOCD1 (P240S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2344004	NM_144569.7(SPOCD1):c.2783G>C (p.Cys928Ser)	SPOCD1 (C234S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2561533	NM_144569.7(SPOCD1):c.2597C>A (p.Pro866His)	SPOCD1 (P130H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208873	NM_144569.7(SPOCD1):c.2531A>G (p.Asp844Gly)	SPOCD1 (D150G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528341	NM_144569.7(SPOCD1):c.2293T>C (p.Cys765Arg)	SPOCD1 (C71R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3322322	NM_144569.7(SPOCD1):c.2267T>C (p.Leu756Pro)	SPOCD1 (L756P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3169265	NM_144569.7(SPOCD1):c.2242G>A (p.Asp748Asn)	SPOCD1 (D241N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2612324	NM_144569.7(SPOCD1):c.2201A>T (p.Lys734Ile)	SPOCD1 (K40I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2626780	NM_144569.7(SPOCD1):c.1991_1992del (p.Arg664fs)	SPOCD1 (R157fs +1 more)	Deletion (frameshift variant +1 more)	Male infertility with azoospermia or oligozoospermia due to single gene mutation	GLikely pathogenic
Select item 2380308	NM_144569.7(SPOCD1):c.1931T>C (p.Ile644Thr)	SPOCD1 (I137T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2286898	NM_144569.7(SPOCD1):c.1885G>C (p.Asp629His)	SPOCD1 (D629H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411707	NM_144569.7(SPOCD1):c.1873C>T (p.Arg625Trp)	SPOCD1 (R118W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3322319	NM_144569.7(SPOCD1):c.1841G>A (p.Arg614His)	SPOCD1 (R107H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2367117	NM_144569.7(SPOCD1):c.1840C>T (p.Arg614Cys)	SPOCD1 (R614C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518493	NM_144569.7(SPOCD1):c.1832C>T (p.Thr611Ile)	SPOCD1 (T104I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3169264	NM_144569.7(SPOCD1):c.1808C>T (p.Ser603Phe)	SPOCD1 (S96F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589354	NM_144569.7(SPOCD1):c.1763C>T (p.Pro588Leu)	SPOCD1 (P588L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3169263	NM_144569.7(SPOCD1):c.1615T>C (p.Ser539Pro)	SPOCD1 (S32P +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 786757	NM_144569.7(SPOCD1):c.1557C>T (p.Leu519=)	SPOCD1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2376482	NM_144569.7(SPOCD1):c.1480G>C (p.Gly494Arg)	SPOCD1 (G494R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495913	NM_144569.7(SPOCD1):c.1399C>G (p.Pro467Ala)	SPOCD1 (P467A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2612435	NM_144569.7(SPOCD1):c.1376C>G (p.Pro459Arg)	SPOCD1 (P459R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380307	NM_144569.7(SPOCD1):c.1364C>T (p.Pro455Leu)	SPOCD1 (P455L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3169262	NM_144569.7(SPOCD1):c.1307G>A (p.Arg436Gln)	SPOCD1 (R436Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2272917	NM_144569.7(SPOCD1):c.1264A>T (p.Thr422Ser)	SPOCD1 (T422S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304832	NM_144569.7(SPOCD1):c.1240A>G (p.Met414Val)	SPOCD1 (M414V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3322312	NM_144569.7(SPOCD1):c.1239C>A (p.Phe413Leu)	SPOCD1 (F413L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3169261	NM_144569.7(SPOCD1):c.1225T>A (p.Cys409Ser)	SPOCD1 (C409S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385208	NM_144569.7(SPOCD1):c.1216A>G (p.Ser406Gly)	SPOCD1 (S406G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3169259	NM_144569.7(SPOCD1):c.1205A>T (p.Asp402Val)	SPOCD1 (D402V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458316	NM_144569.7(SPOCD1):c.1171C>T (p.Arg391Trp)	SPOCD1 (R391W)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2215470	NM_144569.7(SPOCD1):c.1141G>A (p.Ala381Thr)	SPOCD1 (A381T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2312787	NM_144569.7(SPOCD1):c.1090C>A (p.Leu364Met)	SPOCD1 (L364M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3322318	NM_144569.7(SPOCD1):c.1056T>G (p.Asp352Glu)	SPOCD1 (D352E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3169272	NM_144569.7(SPOCD1):c.995C>T (p.Ala332Val)	SPOCD1 (A332V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3169271	NM_144569.7(SPOCD1):c.994G>A (p.Ala332Thr)	SPOCD1 (A332T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3169270	NM_144569.7(SPOCD1):c.908C>G (p.Pro303Arg)	SPOCD1 (P303R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234821	NM_144569.7(SPOCD1):c.908C>T (p.Pro303Leu)	SPOCD1 (P303L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384931	NM_144569.7(SPOCD1):c.877G>C (p.Asp293His)	SPOCD1 (D293H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458843	NM_144569.7(SPOCD1):c.868G>A (p.Ala290Thr)	SPOCD1 (A290T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342100	NM_144569.7(SPOCD1):c.866C>G (p.Pro289Arg)	SPOCD1 (P289R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 717760	NM_144569.7(SPOCD1):c.745C>G (p.Leu249Val)	SPOCD1 (L249V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3322317	NM_144569.7(SPOCD1):c.742G>A (p.Asp248Asn)	SPOCD1 (D248N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 775531	NM_144569.7(SPOCD1):c.732C>G (p.Pro244=)	SPOCD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2552669	NM_144569.7(SPOCD1):c.727C>A (p.Pro243Thr)	SPOCD1 (P243T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3169269	NM_144569.7(SPOCD1):c.688C>G (p.Gln230Glu)	SPOCD1 (Q230E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3322320	NM_144569.7(SPOCD1):c.675C>G (p.Phe225Leu)	SPOCD1 (F225L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589529	NM_144569.7(SPOCD1):c.629G>A (p.Arg210Lys)	SPOCD1 (R210K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376767	NM_144569.7(SPOCD1):c.620A>G (p.Lys207Arg)	SPOCD1 (K207R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301100	NM_144569.7(SPOCD1):c.562G>A (p.Glu188Lys)	SPOCD1 (E188K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232638	NM_144569.7(SPOCD1):c.521C>A (p.Ser174Tyr)	SPOCD1 (S174Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590520	NM_144569.7(SPOCD1):c.461C>A (p.Ala154Glu)	SPOCD1 (A154E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3322321	NM_144569.7(SPOCD1):c.428C>T (p.Pro143Leu)	SPOCD1 (P143L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2562463	NM_144569.7(SPOCD1):c.317C>T (p.Ser106Leu)	SPOCD1 (S106L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472642	NM_144569.7(SPOCD1):c.242G>A (p.Gly81Glu)	SPOCD1 (G81E)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2214395	NM_144569.7(SPOCD1):c.235C>T (p.Arg79Trp)	SPOCD1 (R79W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599139	NM_144569.7(SPOCD1):c.212G>A (p.Arg71Gln)	SPOCD1 (R71Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2301211	NM_144569.7(SPOCD1):c.161G>T (p.Gly54Val)	SPOCD1 (G54V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2354462	NM_144569.7(SPOCD1):c.148G>A (p.Gly50Arg)	SPOCD1 (G50R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2556897	NM_144569.7(SPOCD1):c.110G>T (p.Gly37Val)	SPOCD1 (G37V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3169258	NM_144569.7(SPOCD1):c.11C>T (p.Ala4Val)	SPOCD1 (A4V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 85