ClinVar for Gene (Select 151556) - ClinVar

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Links from Gene

Items: 92

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282274	NM_152529.7(GPR155):c.1868T>C (p.Phe623Ser)	GPR155 (F623S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282273	NM_152529.7(GPR155):c.708G>T (p.Lys236Asn)	GPR155 (K236N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282272	NM_152529.7(GPR155):c.2060G>A (p.Arg687Lys)	GPR155 (R687K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282271	NM_152529.7(GPR155):c.2224C>A (p.Pro742Thr)	GPR155 (P714T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282270	NM_152529.7(GPR155):c.1696G>A (p.Gly566Arg)	GPR155 (G538R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282269	NM_152529.7(GPR155):c.1969C>G (p.Arg657Gly)	GPR155 (R629G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282268	NM_152529.7(GPR155):c.1022A>G (p.Glu341Gly)	GPR155 (E341G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282267	NM_152529.7(GPR155):c.1892G>C (p.Ser631Thr)	GPR155 (S631T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282266	NM_152529.7(GPR155):c.353G>A (p.Cys118Tyr)	GPR155 (C118Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282265	NM_152529.7(GPR155):c.99C>A (p.Asp33Glu)	GPR155 (D33E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101529	NM_152529.7(GPR155):c.655A>G (p.Ile219Val)	GPR155 (I219V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101528	NM_152529.7(GPR155):c.645A>T (p.Leu215Phe)	GPR155 (L215F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101527	NM_152529.7(GPR155):c.2276G>A (p.Arg759His)	GPR155 (R759H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101526	NM_152529.7(GPR155):c.197C>T (p.Thr66Ile)	GPR155 (T66I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101525	NM_152529.7(GPR155):c.1555G>A (p.Glu519Lys)	GPR155 (E491K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101524	NM_152529.7(GPR155):c.1447A>G (p.Ile483Val)	GPR155 (I455V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101523	NM_152529.7(GPR155):c.1078G>A (p.Val360Ile)	GPR155 (V360I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620925	NM_152529.7(GPR155):c.2318G>A (p.Gly773Asp)	GPR155 (G745D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613219	NM_152529.7(GPR155):c.2599T>A (p.Ser867Thr)	GPR155 (S839T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610891	NM_152529.7(GPR155):c.1358C>T (p.Ser453Phe)	GPR155 (S425F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600792	NM_152529.7(GPR155):c.428A>T (p.Gln143Leu)	GPR155 (Q143L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600513	NM_152529.7(GPR155):c.774T>G (p.Phe258Leu)	GPR155 (F258L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600468	NM_152529.7(GPR155):c.2539G>A (p.Ala847Thr)	GPR155 (A847T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596362	NM_152529.7(GPR155):c.55A>C (p.Thr19Pro)	GPR155 (T19P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522955	NM_152529.7(GPR155):c.1880A>G (p.Asn627Ser)	GPR155 (N627S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490070	NM_152529.7(GPR155):c.631C>A (p.Leu211Ile)	GPR155 (L211I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489129	NM_152529.7(GPR155):c.619G>T (p.Val207Leu)	GPR155 (V207L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488109	NM_152529.7(GPR155):c.918T>G (p.Ser306Arg)	GPR155 (S306R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473108	NM_152529.7(GPR155):c.2398G>A (p.Gly800Ser)	GPR155 (G772S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393552	NM_152529.7(GPR155):c.1721C>T (p.Pro574Leu)	GPR155 (P546L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388842	NM_152529.7(GPR155):c.1564A>G (p.Ile522Val)	GPR155 (I494V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370623	NM_152529.7(GPR155):c.2291G>A (p.Arg764Gln)	GPR155 (R736Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2358510	NM_152529.7(GPR155):c.2201A>C (p.Asp734Ala)	GPR155 (D734A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350413	NM_152529.7(GPR155):c.1663G>A (p.Asp555Asn)	GPR155 (D555N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340449	NM_152529.7(GPR155):c.1303G>T (p.Val435Phe)	GPR155 (V407F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339762	NM_152529.7(GPR155):c.1501A>C (p.Ile501Leu)	GPR155 (I501L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337047	NM_152529.7(GPR155):c.1240C>T (p.Leu414Phe)	GPR155 (L414F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334857	NM_152529.7(GPR155):c.1592G>A (p.Ser531Asn)	GPR155 (S531N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316844	NM_152529.7(GPR155):c.1315A>T (p.Asn439Tyr)	GPR155 (N439Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314962	NM_152529.7(GPR155):c.697C>G (p.Leu233Val)	GPR155 (L233V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298046	NM_152529.7(GPR155):c.2367G>T (p.Trp789Cys)	GPR155 (W761C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296697	NM_152529.7(GPR155):c.2465A>G (p.Tyr822Cys)	GPR155 (Y794C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293459	NM_152529.7(GPR155):c.2473C>T (p.Arg825Trp)	GPR155 (R797W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292705	NM_152529.7(GPR155):c.1591A>G (p.Ser531Gly)	GPR155 (S503G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291431	NM_152529.7(GPR155):c.1757C>G (p.Ser586Cys)	GPR155 (S586C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289710	NM_152529.7(GPR155):c.2395C>T (p.Arg799Cys)	GPR155 (R771C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272965	NM_152529.7(GPR155):c.887A>C (p.Glu296Ala)	GPR155 (E296A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258078	NM_152529.7(GPR155):c.83T>G (p.Phe28Cys)	GPR155 (F28C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239728	NM_152529.7(GPR155):c.1436T>G (p.Ile479Ser)	GPR155 (I451S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237014	NM_152529.7(GPR155):c.1139A>C (p.Gln380Pro)	GPR155 (Q380P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233998	NM_152529.7(GPR155):c.1996A>G (p.Ile666Val)	GPR155 (I638V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224972	NM_152529.7(GPR155):c.1618A>G (p.Met540Val)	GPR155 (M512V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221045	NM_152529.7(GPR155):c.109A>G (p.Met37Val)	GPR155 (M37V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808725	GRCh37/hg19 2q31.1-31.3(chr2:175143352-180999636)x1	AGPS, ATF2 +38 more	Copy number loss	not provided	GPathogenic
Select item 1703543	GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373)	ABCA12, ABCB11 +1216 more	Copy number gain	Mosaic trisomy 2	GPathogenic
Select item 1695396	Single allele	AGPS, ATF2 +47 more	Deletion	Split hand-foot malformation 5	GPathogenic
Select item 1526933	GRCh37/hg19 2q31.1-35(chr2:169829974-215521436)	AGPS, ANKAR +217 more	Copy number gain	not specified	GPathogenic
Select item 1339874	GRCh37/hg19 2q31.1(chr2:174673094-177275625)x3	ATF2, ATP5MC3 +22 more	Copy number gain	not provided	Gnot provided
Select item 1047877	GRCh37/hg19 2q31.1-31.3(chr2:171999572-182774361)	PJVK, RBM45 +60 more	Copy number loss	3-4 finger osseus syndactyly +1 more	GPathogenic
Select item 981210	GRCh37/hg19 2q24.2-31.3(chr2:163078055-182119617)x1	ABCB11, AGPS +97 more	Copy number loss	2q24 microdeletion syndrome	GPathogenic
Select item 814347	GRCh37/hg19 2q31.1-32.3(chr2:174690039-195521582)x1	AGPS, ANKAR +86 more	Copy number loss	not provided	GPathogenic
Select item 814344	GRCh37/hg19 2q31.1(chr2:173865202-175428639)x1	CDCA7, CIR1 +8 more	Copy number loss	not provided	GUncertain significance
Select item 814337	GRCh37/hg19 2q24.2-34(chr2:163233162-211927188)x3	CASP8, CAVIN2 +233 more	Copy number gain	not provided	GPathogenic
Select item 781686	NM_152529.7(GPR155):c.2178T>C (p.Leu726=)	GPR155	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 778014	NM_152529.7(GPR155):c.2136A>G (p.Gly712=)	GPR155	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 775787	NM_152529.7(GPR155):c.1596C>T (p.Ile532=)	GPR155	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 730287	NM_152529.7(GPR155):c.479C>T (p.Thr160Ile)	GPR155 (T160I)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 727986	NM_152529.7(GPR155):c.2379C>T (p.Val793=)	GPR155	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 711856	NM_152529.7(GPR155):c.1090T>C (p.Leu364=)	GPR155	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 687517	GRCh37/hg19 2q24.3-32.3(chr2:167329586-192756373)x1	ABCB11, AGPS +125 more	Copy number loss	not provided	GPathogenic
Select item 685829	GRCh37/hg19 2q31.1-32.1(chr2:173538954-186401606)x1	AGPS, ATF2 +56 more	Copy number loss	not provided	GPathogenic
Select item 562670	GRCh37/hg19 2q31.1(chr2:171667051-176832848)x3	ATF2, ATP5MC3 +27 more	Copy number gain	not provided	GPathogenic
Select item 562664	GRCh37/hg19 2q31.1-31.2(chr2:173741558-178416381)x1	AGPS, ATF2 +29 more	Copy number loss	not provided	GPathogenic
Select item 443305	GRCh37/hg19 2q31.1(chr2:174783555-176832848)x1	ATF2, ATP5MC3 +10 more	Copy number loss	See cases	GUncertain significance
Select item 442998	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)	RGPD4, RGPD5 +1214 more	Copy number gain	See cases	GPathogenic
Select item 442997	GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3	IL1F10, IL1R1 +1214 more	Copy number gain	See cases	GPathogenic
Select item 253638	GRCh37/hg19 2q24.1-31.3(chr2:156489430-182921298)x3	ABCB11, ACVR1 +129 more	Copy number gain	See cases	GPathogenic
Select item 253337	GRCh37/hg19 2q31.1(chr2:174586724-176423918)x1	ATF2, ATP5MC3 +9 more	Copy number loss	See cases	GLikely pathogenic
Select item 155530	GRCh38/hg38 2q31.1-31.3(chr2:174236451-181188846)x1	AGPS, ATF2 +224 more	Copy number loss	See cases	GPathogenic
Select item 154811	GRCh38/hg38 2q31.1(chr2:173713838-175467462)x1	ATF2, ATP5MC3 +66 more	Copy number loss	See cases	GPathogenic
Select item 154177	GRCh38/hg38 2q24.1-31.1(chr2:154294042-175989372)x3	LOC129935011, LOC129935012 +530 more	Copy number gain	See cases	GPathogenic
Select item 150849	GRCh38/hg38 2q31.1-31.2(chr2:171513047-177854080)x1	AGPS, ATF2 +214 more	Copy number loss	See cases	GPathogenic
Select item 150325	GRCh38/hg38 2q31.1(chr2:174343200-174549848)x1	CIR1, GPR155 +5 more	Copy number loss	See cases	GUncertain significance
Select item 149687	GRCh38/hg38 2q31.1(chr2:173713838-175467462)x3	ATF2, ATP5MC3 +66 more	Copy number gain	See cases	Gconflicting data from submitters
Select item 147692	GRCh38/hg38 2q31.1-32.2(chr2:171429233-189179568)x1	AGPS, ATF2 +417 more	Copy number loss	See cases	GPathogenic
Select item 60253	GRCh38/hg38 2q31.1-32.1(chr2:170407688-186189894)x1	AGPS, ATF2 +411 more	Copy number loss	See cases	GPathogenic
Select item 60248	GRCh38/hg38 2q24.3-32.1(chr2:163965382-182195062)x1	ABCB11, AGPS +488 more	Copy number loss	See cases	GPathogenic
Select item 58768	GRCh38/hg38 2q31.1(chr2:173699279-175586070)x1	ATF2, ATP5MC3 +68 more	Copy number loss	See cases	GPathogenic
Select item 58767	GRCh38/hg38 2q31.1-31.2(chr2:173408061-177702487)x1	AGPS, ATF2 +150 more	Copy number loss	See cases	GPathogenic
Select item 58766	GRCh38/hg38 2q31.1(chr2:172366752-176361187)x1	ATF2, ATP5MC3 +136 more	Copy number loss	See cases	GPathogenic
Select item 57491	GRCh38/hg38 2q24.3-31.1(chr2:164850117-175559190)x1	ABCB11, ATF2 +269 more	Copy number loss	See cases	GPathogenic
Select item 57130	GRCh38/hg38 2q31.1-31.2(chr2:172779876-177598000)x1	ATP5MC3, ATF2 +159 more	Copy number loss	See cases	GPathogenic

ClinVar

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Links from Gene

Items: 92