GPRC5A[gene] - ClinVar

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Items: 72

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151004	GRCh38/hg38 12p13.33-11.1(chr12:54427-34608071)x4	TAS2R9, TEAD4 +1258 more	Copy number gain	See cases	GPathogenic
Select item 153962	GRCh38/hg38 12p13.33-11.1(chr12:64620-34682902)x4	CLEC12A, CLEC12A-AS1 +1258 more	Copy number gain	See cases	GPathogenic
Select item 59794	GRCh38/hg38 12p13.33-11.1(chr12:77187-34380176)x3	LOC126861410, LOC126861411 +1258 more	Copy number gain	See cases	GPathogenic
Select item 59795	GRCh38/hg38 12p13.33-12.1(chr12:80412-25470329)x3	A2M, A2M-AS1 +1009 more	Copy number gain	See cases	GPathogenic
Select item 147419	GRCh38/hg38 12p13.33-11.1(chr12:121255-34603274)x3	LOC130007230, LOC130007231 +1257 more	Copy number gain	See cases	GPathogenic
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	ACAD10, ACADS +4836 more	Copy number gain	See cases	GPathogenic
Select item 150158	GRCh38/hg38 12p13.33-11.1(chr12:121271-34603261)x3	LOC126861494, LOC126861495 +1257 more	Copy number gain	See cases	GPathogenic
Select item 59799	GRCh38/hg38 12p13.33-11.1(chr12:212976-33926913)x4	CACNA1C-AS2, CACNA1C-AS4 +1242 more	Copy number gain	See cases	GPathogenic
Select item 153563	GRCh38/hg38 12p13.33-12.2(chr12:1258274-20657577)x3	A2M, A2M-AS1 +853 more	Copy number gain	See cases	GPathogenic
Select item 148626	GRCh38/hg38 12p13.33-12.3(chr12:2871741-14987348)x3	LOC130007190, LOC130007191 +698 more	Copy number gain	See cases	GPathogenic
Select item 154815	GRCh38/hg38 12p13.2-12.3(chr12:11121039-15908154)x1	APOLD1, ARHGDIB +238 more	Copy number loss	See cases	GLikely pathogenic
Select item 57166	GRCh38/hg38 12p13.2-13.1(chr12:11771233-13547775)x1	APOLD1, BCL2L14 +121 more	Copy number loss	See cases	GPathogenic
Select item 146005	GRCh38/hg38 12p13.2-12.3(chr12:12363649-15280588)x1	APOLD1, ARHGDIB +137 more	Copy number loss	See cases	GPathogenic
Select item 58986	GRCh38/hg38 12p13.2-12.3(chr12:12388842-15540422)x1	APOLD1, ARHGDIB +140 more	Copy number loss	See cases	GPathogenic
Select item 3282484	NM_003979.4(GPRC5A):c.28C>T (p.Arg10Cys)	GPRC5A (R10C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781065	NM_003979.4(GPRC5A):c.71C>G (p.Ala24Gly)	GPRC5A (A24G)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3101955	NM_003979.4(GPRC5A):c.98C>T (p.Thr33Met)	GPRC5A (T33M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 722961	NM_003979.4(GPRC5A):c.99G>A (p.Thr33=)	GPRC5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2457095	NM_003979.4(GPRC5A):c.112G>A (p.Gly38Arg)	GPRC5A (G38R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357079	NM_003979.4(GPRC5A):c.137T>C (p.Met46Thr)	GPRC5A (M46T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287819	NM_003979.4(GPRC5A):c.173A>G (p.Asp58Gly)	GPRC5A (D58G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101951	NM_003979.4(GPRC5A):c.185G>A (p.Arg62Gln)	GPRC5A (R62Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384892	NM_003979.4(GPRC5A):c.245C>T (p.Thr82Ile)	GPRC5A (T82I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2642741	NM_003979.4(GPRC5A):c.258C>T (p.Ile86=)	GPRC5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3282482	NM_003979.4(GPRC5A):c.271G>A (p.Gly91Arg)	GPRC5A (G91R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525415	NM_003979.4(GPRC5A):c.275G>C (p.Ser92Thr)	GPRC5A (S92T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101952	NM_003979.4(GPRC5A):c.335T>C (p.Leu112Pro)	GPRC5A (L112P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512890	NM_003979.4(GPRC5A):c.520A>C (p.Asn174His)	GPRC5A (N174H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471715	NM_003979.4(GPRC5A):c.520A>T (p.Asn174Tyr)	GPRC5A (N174Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2642742	NM_003979.4(GPRC5A):c.544A>G (p.Thr182Ala)	GPRC5A (T182A)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 722733	NM_003979.4(GPRC5A):c.693C>T (p.Leu231=)	GPRC5A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2405272	NM_003979.4(GPRC5A):c.742G>A (p.Ala248Thr)	GPRC5A (A248T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404202	NM_003979.4(GPRC5A):c.755A>G (p.Asn252Ser)	GPRC5A (N252S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598657	NM_003979.4(GPRC5A):c.763G>A (p.Val255Met)	GPRC5A (V255M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101953	NM_003979.4(GPRC5A):c.775G>T (p.Ala259Ser)	GPRC5A (A259S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520787	NM_003979.4(GPRC5A):c.815G>A (p.Arg272Gln)	GPRC5A (R272Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3282485	NM_003979.4(GPRC5A):c.838G>C (p.Glu280Gln)	GPRC5A (E280Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101954	NM_003979.4(GPRC5A):c.930A>T (p.Glu310Asp)	GPRC5A (E310D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474151	NM_003979.4(GPRC5A):c.932A>G (p.Glu311Gly)	GPRC5A (E311G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101950	NM_003979.4(GPRC5A):c.1028G>T (p.Trp343Leu)	GPRC5A (W343L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282483	NM_003979.4(GPRC5A):c.1049A>G (p.Tyr350Cys)	GPRC5A (Y350C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459092	NM_003979.4(GPRC5A):c.1067G>A (p.Gly356Asp)	GPRC5A (G356D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063250	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835641)x3	A2M, A2ML1 +278 more	Copy number gain	not specified	GPathogenic
Select item 2671607	Single allele	FGD4, FGF23 +278 more	Duplication	not provided	GPathogenic
Select item 2506545	GRCh37/hg19 12p13.2-13.1(chr12:11463270-14019142)	APOLD1, BCL2L14 +19 more	Copy number loss	Intellectual disability	GPathogenic
Select item 2445417	GRCh37/hg19 12p13.33-11.1(chr12:176047-34179852)x4	DENND5B, DERA +278 more	Copy number gain	Pallister-Killian syndrome	GPathogenic
Select item 1711362	GRCh37/hg19 12p13.2-12.1(chr12:10853887-24103810)x1	C12orf60, YBX3 +85 more	Copy number loss	not provided	GPathogenic
Select item 1527672	GRCh37/hg19 12p13.33-q11(chr12:173786-37869301)	C3AR1, CACNA1C +278 more	Copy number gain	not specified	GPathogenic
Select item 1527671	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)	A2M, A2ML1 +278 more	Copy number gain	not specified	GPathogenic
Select item 1527669	GRCh37/hg19 12p13.33-12.1(chr12:173786-25286865)	A2ML1, ABCC9 +235 more	Copy number gain	not specified	GPathogenic
Select item 1436741	NC_000012.11:g.(?_11803062)_(15835885_?)dup	APOLD1, ARHGDIB +32 more	Duplication	Developmental and epileptic encephalopathy, 27 +1 more	GUncertain significance
Select item 831584	NC_000012.12:g.(?_12717002)_(13982130_?)del	APOLD1, CDKN1B +8 more	Deletion	Developmental and epileptic encephalopathy, 27 +1 more	GPathogenic
Select item 831573	NC_000012.12:g.(?_12717002)_(13982130_?)dup	APOLD1, CDKN1B +8 more	Duplication	Developmental and epileptic encephalopathy, 27 +1 more	GUncertain significance
Select item 815505	GRCh37/hg19 12p13.2-12.3(chr12:11737824-16780886)x1	APOLD1, ARHGDIB +37 more	Copy number loss	not provided	GPathogenic
Select item 815493	GRCh37/hg19 12p13.33-q11(chr12:274676-37869301)x4	ART4, DYRK4 +278 more	Copy number gain	not provided	GPathogenic
Select item 686501	GRCh37/hg19 12p13.33-11.1(chr12:173786-34496628)x3	CLEC1B, CLEC2A +278 more	Copy number gain	not provided	GPathogenic
Select item 625809	GRCh37/hg19 12p13.33-12.3(chr12:189216-15001420)	A2M, A2ML1 +193 more	Copy number gain	not provided	GPathogenic
Select item 625596	GRCh37/hg19 12p13.2-13.1(chr12:10336209-13535349)	APOLD1, BCL2L14 +47 more	Copy number loss	Multiple endocrine neoplasia type 4	GPathogenic
Select item 563991	GRCh37/hg19 12p13.33-q11(chr12:173786-37869107)x3	A2M, A2ML1 +278 more	Copy number gain	not provided	GPathogenic
Select item 563990	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x3	A2M, A2ML1 +278 more	Copy number gain	not provided	GPathogenic
Select item 563989	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x2,3	A2M, A2ML1 +278 more	Copy number gain	not provided	GPathogenic
Select item 563981	GRCh37/hg19 12p13.2-13.1(chr12:10717428-14032860)x1	APOLD1, BCL2L14 +40 more	Copy number loss	not provided	GPathogenic
Select item 443532	GRCh37/hg19 12p13.33-11.22(chr12:173786-28219229)x3	A2M, A2ML1 +256 more	Copy number gain	See cases	GPathogenic
Select item 442150	GRCh37/hg19 12p13.33-11.1(chr12:565369-34835837)x3	KCNA6, KCNJ8 +273 more	Copy number gain	See cases	GLikely pathogenic
Select item 441984	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	SLC15A5, SLC16A7 +1006 more	Copy number gain	See cases	GPathogenic
Select item 441983	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	A2M, A2ML1 +1006 more	Copy number gain	See cases	GPathogenic
Select item 395673	GRCh37/hg19 12p13.33-11.1(chr12:189578-34756150)	A2M, A2ML1 +278 more	Copy number gain	See cases	GPathogenic
Select item 268075	GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3	GALNT8, H2AJ +1007 more	Copy number gain	See cases	GPathogenic
Select item 253582	GRCh37/hg19 12p13.33-11.1(chr12:148034-34178799)x4	ACSM4, CCND2 +278 more	Copy number gain	See cases	GPathogenic
Select item 253493	GRCh37/hg19 12p13.33-11.1(chr12:89061-34178799)x3	A2M, A2ML1 +278 more	Copy number gain	See cases	GPathogenic
Select item 221389	GRCh37/hg19 12p13.2-13.1(chr12:12419642-13256423)x3	APOLD1, BORCS5 +12 more	Copy number gain	Breast ductal adenocarcinoma	GUncertain significance
Select item 221369	chr12:10074776-18800953 complex variant	APOLD1, ARHGDIB +79 more	Complex	Breast ductal adenocarcinoma	GUncertain significance

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Items: 72