PRC1-AS1[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 71

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154848	GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3	LOC130057927, LOC130057928 +1764 more	Copy number gain	See cases	GPathogenic
Select item 154952	GRCh38/hg38 15q23-26.3(chr15:72154949-101920998)x3	LOC116268473, LOC116268474 +1244 more	Copy number gain	See cases	GPathogenic
Select item 147691	GRCh38/hg38 15q25.2-26.3(chr15:82859676-101810992)x3	LOC130057943, LOC130057944 +664 more	Copy number gain	See cases	GPathogenic
Select item 146595	GRCh38/hg38 15q25.2-26.3(chr15:83711377-101843270)x3	LOC130057907, LOC130057908 +630 more	Copy number gain	See cases	GPathogenic
Select item 58580	GRCh38/hg38 15q25.2-26.3(chr15:84169153-101904929)x3	ABHD2, ACAN +611 more	Copy number gain	See cases	GPathogenic
Select item 153554	GRCh38/hg38 15q25.3-26.3(chr15:85397539-101888909)x3	ABHD2, ACAN +552 more	Copy number gain	See cases	GPathogenic
Select item 148189	GRCh38/hg38 15q25.3-26.3(chr15:85826665-101920998)x4	MIR11181, MIR1179 +517 more	Copy number gain	See cases	GPathogenic
Select item 146259	GRCh38/hg38 15q25.3-26.3(chr15:87904735-101843270)x3	LOC130057997, LOC130057998 +500 more	Copy number gain	See cases	GPathogenic
Select item 154660	GRCh38/hg38 15q26.1-26.3(chr15:88676575-98364743)x3	LOC130057929, LOC130057930 +311 more	Copy number gain	See cases	GPathogenic
Select item 58582	GRCh38/hg38 15q26.1-26.3(chr15:89679237-101978958)x3	ADAMTS17, ALDH1A3 +422 more	Copy number gain	See cases	GPathogenic
Select item 157650	NM_003981.4(PRC1):c.*733G>A	PRC1, PRC1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 157645	NM_003981.4(PRC1):c.*627T>C	PRC1, PRC1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 157649	NM_003981.4(PRC1):c.*441C>A	PRC1, PRC1-AS1	Single nucleotide variant (3 prime UTR variant)	Familial cancer of breast	GUncertain significance
Select item 157648	NM_003981.4(PRC1):c.*342A>G	PRC1, PRC1-AS1	Single nucleotide variant (3 prime UTR variant)	Familial cancer of breast	GUncertain significance
Select item 2491346	NM_003981.4(PRC1):c.1802C>T (p.Ser601Leu)	PRC1-AS1, PRC1 (S587L +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 157644	NM_003981.4(PRC1):c.1792-828T>C	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 2622271	NM_003981.4(PRC1):c.1755T>G (p.Asp585Glu)	PRC1, PRC1-AS1 (D585E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362018	NM_003981.4(PRC1):c.1739C>T (p.Ser580Phe)	PRC1, PRC1-AS1 (S580F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311592	NM_003981.4(PRC1):c.1703G>A (p.Arg568His)	PRC1, PRC1-AS1 (R568H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376487	NM_003981.4(PRC1):c.1672G>T (p.Gly558Cys)	PRC1, PRC1-AS1 (A517S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599345	NM_003981.4(PRC1):c.1657G>A (p.Gly553Ser)	PRC1, PRC1-AS1 (G553S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218294	NM_003981.4(PRC1):c.1635C>G (p.Asn545Lys)	PRC1, PRC1-AS1 (N504K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218293	NM_003981.4(PRC1):c.1619G>A (p.Gly540Asp)	PRC1, PRC1-AS1 (G540D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309722	NM_003981.4(PRC1):c.1612C>T (p.Arg538Cys)	PRC1, PRC1-AS1 (R497C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218292	NM_003981.4(PRC1):c.1559C>T (p.Pro520Leu)	PRC1, PRC1-AS1 (P479L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218291	NM_003981.4(PRC1):c.1553T>G (p.Leu518Arg)	PRC1, PRC1-AS1 (L477R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2565419	NM_003981.4(PRC1):c.1550G>A (p.Arg517Gln)	PRC1, PRC1-AS1 (R517Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2567606	NM_003981.4(PRC1):c.1543G>A (p.Val515Met)	PRC1, PRC1-AS1 (V474M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 157643	NM_003981.4(PRC1):c.1532A>G (p.Tyr511Cys)	PRC1, PRC1-AS1 (Y470C +1 more)	Single nucleotide variant (missense variant)	Familial cancer of breast	GUncertain significance
Select item 2366876	NM_003981.4(PRC1):c.1507C>T (p.Arg503Trp)	PRC1, PRC1-AS1 (R462W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218290	NM_003981.4(PRC1):c.1496A>G (p.Asn499Ser)	PRC1, PRC1-AS1 (N458S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 157642	NM_003981.4(PRC1):c.1462-1016G>A	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Breast carcinoma	Gassociation
Select item 3309720	NM_003981.4(PRC1):c.1457G>T (p.Arg486Leu)	PRC1, PRC1-AS1 (R445L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473088	NM_003981.4(PRC1):c.1423C>G (p.Arg475Gly)	PRC1, PRC1-AS1 (R434G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219724	NM_003981.4(PRC1):c.1406G>A (p.Arg469Gln)	PRC1, PRC1-AS1 (R469Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 157641	NM_003981.4(PRC1):c.1351-3C>T	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 157647	NM_003981.3(PRC1):c.1351-124_1351-123insoAC068831.17:g.63209_63266	PRC1, PRC1-AS1	Insertion	Familial cancer of breast	GUncertain significance
Select item 157640	NM_003981.4(PRC1):c.1350+35C>G	PRC1-AS1, PRC1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 2617635	NM_003981.4(PRC1):c.1331A>G (p.Glu444Gly)	PRC1, PRC1-AS1 (E444G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218289	NM_003981.4(PRC1):c.1318C>G (p.Arg440Gly)	PRC1, PRC1-AS1 (R399G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218288	NM_003981.4(PRC1):c.1266G>A (p.Met422Ile)	PRC1, PRC1-AS1 (M381I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309719	NM_003981.4(PRC1):c.1235T>C (p.Leu412Ser)	PRC1, PRC1-AS1 (L371S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464523	NM_003981.4(PRC1):c.1034A>G (p.Tyr345Cys)	PRC1, PRC1-AS1 (Y304C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359130	NM_003981.4(PRC1):c.1018C>T (p.Arg340Trp)	PRC1, PRC1-AS1 (R340W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 710276	NM_003981.4(PRC1):c.971-4G>A	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 157639	NM_003981.4(PRC1):c.971-375A>G	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 157638	NM_003981.4(PRC1):c.971-441G>A	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 157637	NM_003981.4(PRC1):c.971-442C>T	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Breast carcinoma	Gassociation
Select item 157636	NM_003981.4(PRC1):c.971-466T>C	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 157635	NM_003981.4(PRC1):c.970+436G>A	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 2593095	NM_003981.4(PRC1):c.935A>G (p.Gln312Arg)	PRC1, PRC1-AS1 (Q271R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218298	NM_003981.4(PRC1):c.896T>C (p.Val299Ala)	PRC1, PRC1-AS1 (V299A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411963	NM_003981.4(PRC1):c.893G>A (p.Arg298Gln)	PRC1, PRC1-AS1 (R257Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218297	NM_003981.4(PRC1):c.875A>C (p.Lys292Thr)	PRC1, PRC1-AS1 (K292T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595210	NM_003981.4(PRC1):c.863A>G (p.Gln288Arg)	PRC1, PRC1-AS1 (Q247R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487226	NM_003981.4(PRC1):c.742G>A (p.Asp248Asn)	PRC1, PRC1-AS1 (D207N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211139	NM_003981.4(PRC1):c.719G>A (p.Arg240His)	PRC1, PRC1-AS1 (R240H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309723	NM_003981.4(PRC1):c.712G>A (p.Gly238Arg)	PRC1, PRC1-AS1 (G197R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354421	NM_003981.4(PRC1):c.680T>C (p.Met227Thr)	PRC1, PRC1-AS1 (M186T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233983	NM_003981.4(PRC1):c.667C>T (p.Arg223Trp)	PRC1, PRC1-AS1 (R182W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208889	NM_003981.4(PRC1):c.644T>C (p.Ile215Thr)	PRC1, PRC1-AS1 (I215T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252320	NM_003981.4(PRC1):c.613G>A (p.Glu205Lys)	PRC1, PRC1-AS1 (E205K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309569	NM_003981.4(PRC1):c.440T>C (p.Val147Ala)	PRC1, PRC1-AS1 (V106A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511961	NM_003981.4(PRC1):c.332G>A (p.Arg111Gln)	PRC1, PRC1-AS1 (R70Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 157632	NM_003981.4(PRC1):c.282G>A (p.Thr94=)	PRC1-AS1, PRC1	Single nucleotide variant (non-coding transcript variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 157634	NM_003981.4(PRC1):c.268-107G>A	PRC1, PRC1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 157633	NM_003981.4(PRC1):c.268-203A>G	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 2544012	NM_003981.4(PRC1):c.233C>T (p.Thr78Ile)	LOC126862223, PRC1 +1 more (T78I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 157630	NM_003981.4(PRC1):c.145-81A>T	LOC126862223, PRC1 +1 more	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 3218287	NM_003981.4(PRC1):c.113A>G (p.Gln38Arg)	PRC1, PRC1-AS1 (Q38R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 157631	NM_003981.4(PRC1):c.12-2765T>C	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	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: 71