Name: rs1491583420
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs1491583420

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:123345762-123345764 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: dupCA / insCACA / ins(CA)₃ / ins(C…
dupCA / insCACA / ins(CA)₃ / ins(CA)₄ / ins(CA)₅ / ins(CA)₆ / ins(CA)₇ / ins(CA)₈ / ins(CA)₉ / ins(CA)₁₀ / ins(CA)₁₁ / ins(CA)₁₂ / ins(CA)₁₃
Variation Type: Indel Insertion and Deletion
Frequency: dupCA=0.00000 (0/11802, ALFA)
insCACA=0.00000 (0/11802, ALFA)
ins(CA)₃=0.00000 (0/11802, ALFA) (+ 7 more)
ins(CA)₄=0.00000 (0/11802, ALFA)
ins(CA)₅=0.00000 (0/11802, ALFA)
ins(CA)₆=0.00000 (0/11802, ALFA)
ins(CA)₇=0.00000 (0/11802, ALFA)
ins(CA)₈=0.00000 (0/11802, ALFA)
ins(CA)₁₀=0.00000 (0/11802, ALFA)
ins(CA)₁₁=0.00000 (0/11802, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ADCY5 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	11802	ACA=1.00000	ACACA=0.00000, ACACACA=0.00000, ACACACACA=0.00000, ACACACACACA=0.00000, ACACACACACACA=0.00000, ACACACACACACACA=0.00000, ACACACACACACACACA=0.00000, ACACACACACACACACACA=0.00000, ACACACACACACACACACACACA=0.00000, ACACACACACACACACACACACACA=0.00000	1.0	N/A
European	Sub	7616	ACA=1.0000	ACACA=0.0000, ACACACA=0.0000, ACACACACA=0.0000, ACACACACACA=0.0000, ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000	1.0	N/A
African	Sub	2764	ACA=1.0000	ACACA=0.0000, ACACACA=0.0000, ACACACACA=0.0000, ACACACACACA=0.0000, ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000	1.0	N/A
African Others	Sub	106	ACA=1.000	ACACA=0.000, ACACACA=0.000, ACACACACA=0.000, ACACACACACA=0.000, ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000	1.0	N/A
African American	Sub	2658	ACA=1.0000	ACACA=0.0000, ACACACA=0.0000, ACACACACA=0.0000, ACACACACACA=0.0000, ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACACACACACACACACA=0.0000, ACACACACACACACACACA=0.0000, ACACACACACACACACACACACA=0.0000, ACACACACACACACACACACACACA=0.0000	1.0	N/A
Asian	Sub	108	ACA=1.000	ACACA=0.000, ACACACA=0.000, ACACACACA=0.000, ACACACACACA=0.000, ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000	1.0	N/A
East Asian	Sub	84	ACA=1.00	ACACA=0.00, ACACACA=0.00, ACACACACA=0.00, ACACACACACA=0.00, ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00	1.0	N/A
Other Asian	Sub	24	ACA=1.00	ACACA=0.00, ACACACA=0.00, ACACACACA=0.00, ACACACACACA=0.00, ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00	1.0	N/A
Latin American 1	Sub	144	ACA=1.000	ACACA=0.000, ACACACA=0.000, ACACACACA=0.000, ACACACACACA=0.000, ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000	1.0	N/A
Latin American 2	Sub	610	ACA=1.000	ACACA=0.000, ACACACA=0.000, ACACACACA=0.000, ACACACACACA=0.000, ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000	1.0	N/A
South Asian	Sub	94	ACA=1.00	ACACA=0.00, ACACACA=0.00, ACACACACA=0.00, ACACACACACA=0.00, ACACACACACACA=0.00, ACACACACACACACA=0.00, ACACACACACACACACA=0.00, ACACACACACACACACACA=0.00, ACACACACACACACACACACACA=0.00, ACACACACACACACACACACACACA=0.00	1.0	N/A
Other	Sub	466	ACA=1.000	ACACA=0.000, ACACACA=0.000, ACACACACA=0.000, ACACACACACA=0.000, ACACACACACACA=0.000, ACACACACACACACA=0.000, ACACACACACACACACA=0.000, ACACACACACACACACACA=0.000, ACACACACACACACACACACACA=0.000, ACACACACACACACACACACACACA=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	11802	ACA=1.00000	dupCA=0.00000, insCACA=0.00000, ins(CA)₃=0.00000, ins(CA)₄=0.00000, ins(CA)₅=0.00000, ins(CA)₆=0.00000, ins(CA)₇=0.00000, ins(CA)₈=0.00000, ins(CA)₁₀=0.00000, ins(CA)₁₁=0.00000
Allele Frequency Aggregator	European	Sub	7616	ACA=1.0000	dupCA=0.0000, insCACA=0.0000, ins(CA)₃=0.0000, ins(CA)₄=0.0000, ins(CA)₅=0.0000, ins(CA)₆=0.0000, ins(CA)₇=0.0000, ins(CA)₈=0.0000, ins(CA)₁₀=0.0000, ins(CA)₁₁=0.0000
Allele Frequency Aggregator	African	Sub	2764	ACA=1.0000	dupCA=0.0000, insCACA=0.0000, ins(CA)₃=0.0000, ins(CA)₄=0.0000, ins(CA)₅=0.0000, ins(CA)₆=0.0000, ins(CA)₇=0.0000, ins(CA)₈=0.0000, ins(CA)₁₀=0.0000, ins(CA)₁₁=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	ACA=1.000	dupCA=0.000, insCACA=0.000, ins(CA)₃=0.000, ins(CA)₄=0.000, ins(CA)₅=0.000, ins(CA)₆=0.000, ins(CA)₇=0.000, ins(CA)₈=0.000, ins(CA)₁₀=0.000, ins(CA)₁₁=0.000
Allele Frequency Aggregator	Other	Sub	466	ACA=1.000	dupCA=0.000, insCACA=0.000, ins(CA)₃=0.000, ins(CA)₄=0.000, ins(CA)₅=0.000, ins(CA)₆=0.000, ins(CA)₇=0.000, ins(CA)₈=0.000, ins(CA)₁₀=0.000, ins(CA)₁₁=0.000
Allele Frequency Aggregator	Latin American 1	Sub	144	ACA=1.000	dupCA=0.000, insCACA=0.000, ins(CA)₃=0.000, ins(CA)₄=0.000, ins(CA)₅=0.000, ins(CA)₆=0.000, ins(CA)₇=0.000, ins(CA)₈=0.000, ins(CA)₁₀=0.000, ins(CA)₁₁=0.000
Allele Frequency Aggregator	Asian	Sub	108	ACA=1.000	dupCA=0.000, insCACA=0.000, ins(CA)₃=0.000, ins(CA)₄=0.000, ins(CA)₅=0.000, ins(CA)₆=0.000, ins(CA)₇=0.000, ins(CA)₈=0.000, ins(CA)₁₀=0.000, ins(CA)₁₁=0.000
Allele Frequency Aggregator	South Asian	Sub	94	ACA=1.00	dupCA=0.00, insCACA=0.00, ins(CA)₃=0.00, ins(CA)₄=0.00, ins(CA)₅=0.00, ins(CA)₆=0.00, ins(CA)₇=0.00, ins(CA)₈=0.00, ins(CA)₁₀=0.00, ins(CA)₁₁=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 3	NC_000003.12:g.123345763_123345764dup
GRCh38.p14 chr 3	NC_000003.12:g.123345763CA[3]
GRCh38.p14 chr 3	NC_000003.12:g.123345763CA[4]
GRCh38.p14 chr 3	NC_000003.12:g.123345763CA[5]
GRCh38.p14 chr 3	NC_000003.12:g.123345763CA[6]
GRCh38.p14 chr 3	NC_000003.12:g.123345763CA[7]
GRCh38.p14 chr 3	NC_000003.12:g.123345763CA[8]
GRCh38.p14 chr 3	NC_000003.12:g.123345763CA[9]
GRCh38.p14 chr 3	NC_000003.12:g.123345763CA[10]
GRCh38.p14 chr 3	NC_000003.12:g.123345763CA[11]
GRCh38.p14 chr 3	NC_000003.12:g.123345763CA[12]
GRCh38.p14 chr 3	NC_000003.12:g.123345763CA[13]
GRCh38.p14 chr 3	NC_000003.12:g.123345763CA[14]
GRCh37.p13 chr 3	NC_000003.11:g.123064610_123064611dup
GRCh37.p13 chr 3	NC_000003.11:g.123064610CA[3]
GRCh37.p13 chr 3	NC_000003.11:g.123064610CA[4]
GRCh37.p13 chr 3	NC_000003.11:g.123064610CA[5]
GRCh37.p13 chr 3	NC_000003.11:g.123064610CA[6]
GRCh37.p13 chr 3	NC_000003.11:g.123064610CA[7]
GRCh37.p13 chr 3	NC_000003.11:g.123064610CA[8]
GRCh37.p13 chr 3	NC_000003.11:g.123064610CA[9]
GRCh37.p13 chr 3	NC_000003.11:g.123064610CA[10]
GRCh37.p13 chr 3	NC_000003.11:g.123064610CA[11]
GRCh37.p13 chr 3	NC_000003.11:g.123064610CA[12]
GRCh37.p13 chr 3	NC_000003.11:g.123064610CA[13]
GRCh37.p13 chr 3	NC_000003.11:g.123064610CA[14]
ADCY5 RefSeqGene	NG_033882.1:g.107783_107784dup
ADCY5 RefSeqGene	NG_033882.1:g.107783GT[3]
ADCY5 RefSeqGene	NG_033882.1:g.107783GT[4]
ADCY5 RefSeqGene	NG_033882.1:g.107783GT[5]
ADCY5 RefSeqGene	NG_033882.1:g.107783GT[6]
ADCY5 RefSeqGene	NG_033882.1:g.107783GT[7]
ADCY5 RefSeqGene	NG_033882.1:g.107783GT[8]
ADCY5 RefSeqGene	NG_033882.1:g.107783GT[9]
ADCY5 RefSeqGene	NG_033882.1:g.107783GT[10]
ADCY5 RefSeqGene	NG_033882.1:g.107783GT[11]
ADCY5 RefSeqGene	NG_033882.1:g.107783GT[12]
ADCY5 RefSeqGene	NG_033882.1:g.107783GT[13]
ADCY5 RefSeqGene	NG_033882.1:g.107783GT[14]

Gene: ADCY5, adenylate cyclase 5 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ADCY5 transcript variant 2	NM_001199642.1:c.356+2019… NM_001199642.1:c.356+2019_356+2020dup	N/A	Intron Variant
ADCY5 transcript variant 3	NM_001378259.1:c.1406+201… NM_001378259.1:c.1406+2019_1406+2020dup	N/A	Intron Variant
ADCY5 transcript variant 1	NM_183357.3:c.1406+2019_1… NM_183357.3:c.1406+2019_1406+2020dup	N/A	Intron Variant
ADCY5 transcript variant X3	XM_005247078.1:c.356+2019… XM_005247078.1:c.356+2019_356+2020dup	N/A	Intron Variant
ADCY5 transcript variant X7	XM_006713483.2:c.305+2019… XM_006713483.2:c.305+2019_305+2020dup	N/A	Intron Variant
ADCY5 transcript variant X11	XM_006713484.2:c.83+2019_… XM_006713484.2:c.83+2019_83+2020dup	N/A	Intron Variant
ADCY5 transcript variant X1	XM_011512359.3:c.407+2019… XM_011512359.3:c.407+2019_407+2020dup	N/A	Intron Variant
ADCY5 transcript variant X5	XM_011512360.3:c.317+2019… XM_011512360.3:c.317+2019_317+2020dup	N/A	Intron Variant
ADCY5 transcript variant X12	XM_011512361.2:c.83+2019_… XM_011512361.2:c.83+2019_83+2020dup	N/A	Intron Variant
ADCY5 transcript variant X2	XM_017005638.1:c.308+2019… XM_017005638.1:c.308+2019_308+2020dup	N/A	Intron Variant
ADCY5 transcript variant X6	XM_017005639.1:c.308+2019… XM_017005639.1:c.308+2019_308+2020dup	N/A	Intron Variant
ADCY5 transcript variant X4	XM_047447359.1:c.407+2019… XM_047447359.1:c.407+2019_407+2020dup	N/A	Intron Variant
ADCY5 transcript variant X8	XM_047447360.1:c.317+2019… XM_047447360.1:c.317+2019_317+2020dup	N/A	Intron Variant
ADCY5 transcript variant X9	XM_047447361.1:c.308+2019… XM_047447361.1:c.308+2019_308+2020dup	N/A	Intron Variant
ADCY5 transcript variant X10	XM_047447362.1:c.305+2019… XM_047447362.1:c.305+2019_305+2020dup	N/A	Intron Variant
ADCY5 transcript variant X13	XM_047447363.1:c.83+2019_… XM_047447363.1:c.83+2019_83+2020dup	N/A	Intron Variant
ADCY5 transcript variant X14	XM_047447364.1:c.83+2019_… XM_047447364.1:c.83+2019_83+2020dup	N/A	Intron Variant
ADCY5 transcript variant X15	XM_047447365.1:c.	N/A	Genic Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	ACA=	dupCA	insCACA	ins(CA)₃	ins(CA)₄	ins(CA)₅	ins(CA)₆	ins(CA)₇	ins(CA)₈	ins(CA)₉	ins(CA)₁₀	ins(CA)₁₁	ins(CA)₁₂	ins(CA)₁₃
GRCh38.p14 chr 3	NC_000003.12:g.123345762_123345764=	NC_000003.12:g.123345763_123345764dup	NC_000003.12:g.123345763CA[3]	NC_000003.12:g.123345763CA[4]	NC_000003.12:g.123345763CA[5]	NC_000003.12:g.123345763CA[6]	NC_000003.12:g.123345763CA[7]	NC_000003.12:g.123345763CA[8]	NC_000003.12:g.123345763CA[9]	NC_000003.12:g.123345763CA[10]	NC_000003.12:g.123345763CA[11]	NC_000003.12:g.123345763CA[12]	NC_000003.12:g.123345763CA[13]	NC_000003.12:g.123345763CA[14]
GRCh37.p13 chr 3	NC_000003.11:g.123064609_123064611=	NC_000003.11:g.123064610_123064611dup	NC_000003.11:g.123064610CA[3]	NC_000003.11:g.123064610CA[4]	NC_000003.11:g.123064610CA[5]	NC_000003.11:g.123064610CA[6]	NC_000003.11:g.123064610CA[7]	NC_000003.11:g.123064610CA[8]	NC_000003.11:g.123064610CA[9]	NC_000003.11:g.123064610CA[10]	NC_000003.11:g.123064610CA[11]	NC_000003.11:g.123064610CA[12]	NC_000003.11:g.123064610CA[13]	NC_000003.11:g.123064610CA[14]
ADCY5 RefSeqGene	NG_033882.1:g.107782_107784=	NG_033882.1:g.107783_107784dup	NG_033882.1:g.107783GT[3]	NG_033882.1:g.107783GT[4]	NG_033882.1:g.107783GT[5]	NG_033882.1:g.107783GT[6]	NG_033882.1:g.107783GT[7]	NG_033882.1:g.107783GT[8]	NG_033882.1:g.107783GT[9]	NG_033882.1:g.107783GT[10]	NG_033882.1:g.107783GT[11]	NG_033882.1:g.107783GT[12]	NG_033882.1:g.107783GT[13]	NG_033882.1:g.107783GT[14]
ADCY5 transcript variant 2	NM_001199642.1:c.356+2020=	NM_001199642.1:c.356+2019_356+2020dup	NM_001199642.1:c.356+2020_356+2021insTGTG	NM_001199642.1:c.356+2020_356+2021insTGTGTG	NM_001199642.1:c.356+2020_356+2021insTGTGTGTG	NM_001199642.1:c.356+2020_356+2021insTGTGTGTGTG	NM_001199642.1:c.356+2020_356+2021insTGTGTGTGTGTG	NM_001199642.1:c.356+2020_356+2021insTGTGTGTGTGTGTG	NM_001199642.1:c.356+2020_356+2021insTGTGTGTGTGTGTGTG	NM_001199642.1:c.356+2020_356+2021insTGTGTGTGTGTGTGTGTG	NM_001199642.1:c.356+2020_356+2021insTGTGTGTGTGTGTGTGTGTG	NM_001199642.1:c.356+2020_356+2021insTGTGTGTGTGTGTGTGTGTGTG	NM_001199642.1:c.356+2020_356+2021insTGTGTGTGTGTGTGTGTGTGTGTG	NM_001199642.1:c.356+2020_356+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant 3	NM_001378259.1:c.1406+2020=	NM_001378259.1:c.1406+2019_1406+2020dup	NM_001378259.1:c.1406+2020_1406+2021insTGTG	NM_001378259.1:c.1406+2020_1406+2021insTGTGTG	NM_001378259.1:c.1406+2020_1406+2021insTGTGTGTG	NM_001378259.1:c.1406+2020_1406+2021insTGTGTGTGTG	NM_001378259.1:c.1406+2020_1406+2021insTGTGTGTGTGTG	NM_001378259.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTG	NM_001378259.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTG	NM_001378259.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTG	NM_001378259.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTG	NM_001378259.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTGTG	NM_001378259.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTGTGTG	NM_001378259.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant 1	NM_183357.2:c.1406+2020=	NM_183357.2:c.1406+2019_1406+2020dup	NM_183357.2:c.1406+2020_1406+2021insTGTG	NM_183357.2:c.1406+2020_1406+2021insTGTGTG	NM_183357.2:c.1406+2020_1406+2021insTGTGTGTG	NM_183357.2:c.1406+2020_1406+2021insTGTGTGTGTG	NM_183357.2:c.1406+2020_1406+2021insTGTGTGTGTGTG	NM_183357.2:c.1406+2020_1406+2021insTGTGTGTGTGTGTG	NM_183357.2:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTG	NM_183357.2:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTG	NM_183357.2:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTG	NM_183357.2:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTGTG	NM_183357.2:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTGTGTG	NM_183357.2:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant 1	NM_183357.3:c.1406+2020=	NM_183357.3:c.1406+2019_1406+2020dup	NM_183357.3:c.1406+2020_1406+2021insTGTG	NM_183357.3:c.1406+2020_1406+2021insTGTGTG	NM_183357.3:c.1406+2020_1406+2021insTGTGTGTG	NM_183357.3:c.1406+2020_1406+2021insTGTGTGTGTG	NM_183357.3:c.1406+2020_1406+2021insTGTGTGTGTGTG	NM_183357.3:c.1406+2020_1406+2021insTGTGTGTGTGTGTG	NM_183357.3:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTG	NM_183357.3:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTG	NM_183357.3:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTG	NM_183357.3:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTGTG	NM_183357.3:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTGTGTG	NM_183357.3:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X1	XM_005247077.1:c.1406+2020=	XM_005247077.1:c.1406+2019_1406+2020dup	XM_005247077.1:c.1406+2020_1406+2021insTGTG	XM_005247077.1:c.1406+2020_1406+2021insTGTGTG	XM_005247077.1:c.1406+2020_1406+2021insTGTGTGTG	XM_005247077.1:c.1406+2020_1406+2021insTGTGTGTGTG	XM_005247077.1:c.1406+2020_1406+2021insTGTGTGTGTGTG	XM_005247077.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTG	XM_005247077.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTG	XM_005247077.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTG	XM_005247077.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTG	XM_005247077.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_005247077.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_005247077.1:c.1406+2020_1406+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X3	XM_005247078.1:c.356+2020=	XM_005247078.1:c.356+2019_356+2020dup	XM_005247078.1:c.356+2020_356+2021insTGTG	XM_005247078.1:c.356+2020_356+2021insTGTGTG	XM_005247078.1:c.356+2020_356+2021insTGTGTGTG	XM_005247078.1:c.356+2020_356+2021insTGTGTGTGTG	XM_005247078.1:c.356+2020_356+2021insTGTGTGTGTGTG	XM_005247078.1:c.356+2020_356+2021insTGTGTGTGTGTGTG	XM_005247078.1:c.356+2020_356+2021insTGTGTGTGTGTGTGTG	XM_005247078.1:c.356+2020_356+2021insTGTGTGTGTGTGTGTGTG	XM_005247078.1:c.356+2020_356+2021insTGTGTGTGTGTGTGTGTGTG	XM_005247078.1:c.356+2020_356+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_005247078.1:c.356+2020_356+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_005247078.1:c.356+2020_356+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X3	XM_005247079.1:c.305+2020=	XM_005247079.1:c.305+2019_305+2020dup	XM_005247079.1:c.305+2020_305+2021insTGTG	XM_005247079.1:c.305+2020_305+2021insTGTGTG	XM_005247079.1:c.305+2020_305+2021insTGTGTGTG	XM_005247079.1:c.305+2020_305+2021insTGTGTGTGTG	XM_005247079.1:c.305+2020_305+2021insTGTGTGTGTGTG	XM_005247079.1:c.305+2020_305+2021insTGTGTGTGTGTGTG	XM_005247079.1:c.305+2020_305+2021insTGTGTGTGTGTGTGTG	XM_005247079.1:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTG	XM_005247079.1:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTGTG	XM_005247079.1:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_005247079.1:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_005247079.1:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X7	XM_006713483.2:c.305+2020=	XM_006713483.2:c.305+2019_305+2020dup	XM_006713483.2:c.305+2020_305+2021insTGTG	XM_006713483.2:c.305+2020_305+2021insTGTGTG	XM_006713483.2:c.305+2020_305+2021insTGTGTGTG	XM_006713483.2:c.305+2020_305+2021insTGTGTGTGTG	XM_006713483.2:c.305+2020_305+2021insTGTGTGTGTGTG	XM_006713483.2:c.305+2020_305+2021insTGTGTGTGTGTGTG	XM_006713483.2:c.305+2020_305+2021insTGTGTGTGTGTGTGTG	XM_006713483.2:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTG	XM_006713483.2:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTGTG	XM_006713483.2:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_006713483.2:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_006713483.2:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X11	XM_006713484.2:c.83+2020=	XM_006713484.2:c.83+2019_83+2020dup	XM_006713484.2:c.83+2020_83+2021insTGTG	XM_006713484.2:c.83+2020_83+2021insTGTGTG	XM_006713484.2:c.83+2020_83+2021insTGTGTGTG	XM_006713484.2:c.83+2020_83+2021insTGTGTGTGTG	XM_006713484.2:c.83+2020_83+2021insTGTGTGTGTGTG	XM_006713484.2:c.83+2020_83+2021insTGTGTGTGTGTGTG	XM_006713484.2:c.83+2020_83+2021insTGTGTGTGTGTGTGTG	XM_006713484.2:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTG	XM_006713484.2:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTG	XM_006713484.2:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_006713484.2:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_006713484.2:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X1	XM_011512359.3:c.407+2020=	XM_011512359.3:c.407+2019_407+2020dup	XM_011512359.3:c.407+2020_407+2021insTGTG	XM_011512359.3:c.407+2020_407+2021insTGTGTG	XM_011512359.3:c.407+2020_407+2021insTGTGTGTG	XM_011512359.3:c.407+2020_407+2021insTGTGTGTGTG	XM_011512359.3:c.407+2020_407+2021insTGTGTGTGTGTG	XM_011512359.3:c.407+2020_407+2021insTGTGTGTGTGTGTG	XM_011512359.3:c.407+2020_407+2021insTGTGTGTGTGTGTGTG	XM_011512359.3:c.407+2020_407+2021insTGTGTGTGTGTGTGTGTG	XM_011512359.3:c.407+2020_407+2021insTGTGTGTGTGTGTGTGTGTG	XM_011512359.3:c.407+2020_407+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_011512359.3:c.407+2020_407+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_011512359.3:c.407+2020_407+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X5	XM_011512360.3:c.317+2020=	XM_011512360.3:c.317+2019_317+2020dup	XM_011512360.3:c.317+2020_317+2021insTGTG	XM_011512360.3:c.317+2020_317+2021insTGTGTG	XM_011512360.3:c.317+2020_317+2021insTGTGTGTG	XM_011512360.3:c.317+2020_317+2021insTGTGTGTGTG	XM_011512360.3:c.317+2020_317+2021insTGTGTGTGTGTG	XM_011512360.3:c.317+2020_317+2021insTGTGTGTGTGTGTG	XM_011512360.3:c.317+2020_317+2021insTGTGTGTGTGTGTGTG	XM_011512360.3:c.317+2020_317+2021insTGTGTGTGTGTGTGTGTG	XM_011512360.3:c.317+2020_317+2021insTGTGTGTGTGTGTGTGTGTG	XM_011512360.3:c.317+2020_317+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_011512360.3:c.317+2020_317+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_011512360.3:c.317+2020_317+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X12	XM_011512361.2:c.83+2020=	XM_011512361.2:c.83+2019_83+2020dup	XM_011512361.2:c.83+2020_83+2021insTGTG	XM_011512361.2:c.83+2020_83+2021insTGTGTG	XM_011512361.2:c.83+2020_83+2021insTGTGTGTG	XM_011512361.2:c.83+2020_83+2021insTGTGTGTGTG	XM_011512361.2:c.83+2020_83+2021insTGTGTGTGTGTG	XM_011512361.2:c.83+2020_83+2021insTGTGTGTGTGTGTG	XM_011512361.2:c.83+2020_83+2021insTGTGTGTGTGTGTGTG	XM_011512361.2:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTG	XM_011512361.2:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTG	XM_011512361.2:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_011512361.2:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_011512361.2:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X2	XM_017005638.1:c.308+2020=	XM_017005638.1:c.308+2019_308+2020dup	XM_017005638.1:c.308+2020_308+2021insTGTG	XM_017005638.1:c.308+2020_308+2021insTGTGTG	XM_017005638.1:c.308+2020_308+2021insTGTGTGTG	XM_017005638.1:c.308+2020_308+2021insTGTGTGTGTG	XM_017005638.1:c.308+2020_308+2021insTGTGTGTGTGTG	XM_017005638.1:c.308+2020_308+2021insTGTGTGTGTGTGTG	XM_017005638.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTG	XM_017005638.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTG	XM_017005638.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTGTG	XM_017005638.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_017005638.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_017005638.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X6	XM_017005639.1:c.308+2020=	XM_017005639.1:c.308+2019_308+2020dup	XM_017005639.1:c.308+2020_308+2021insTGTG	XM_017005639.1:c.308+2020_308+2021insTGTGTG	XM_017005639.1:c.308+2020_308+2021insTGTGTGTG	XM_017005639.1:c.308+2020_308+2021insTGTGTGTGTG	XM_017005639.1:c.308+2020_308+2021insTGTGTGTGTGTG	XM_017005639.1:c.308+2020_308+2021insTGTGTGTGTGTGTG	XM_017005639.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTG	XM_017005639.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTG	XM_017005639.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTGTG	XM_017005639.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_017005639.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_017005639.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X4	XM_047447359.1:c.407+2020=	XM_047447359.1:c.407+2019_407+2020dup	XM_047447359.1:c.407+2020_407+2021insTGTG	XM_047447359.1:c.407+2020_407+2021insTGTGTG	XM_047447359.1:c.407+2020_407+2021insTGTGTGTG	XM_047447359.1:c.407+2020_407+2021insTGTGTGTGTG	XM_047447359.1:c.407+2020_407+2021insTGTGTGTGTGTG	XM_047447359.1:c.407+2020_407+2021insTGTGTGTGTGTGTG	XM_047447359.1:c.407+2020_407+2021insTGTGTGTGTGTGTGTG	XM_047447359.1:c.407+2020_407+2021insTGTGTGTGTGTGTGTGTG	XM_047447359.1:c.407+2020_407+2021insTGTGTGTGTGTGTGTGTGTG	XM_047447359.1:c.407+2020_407+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_047447359.1:c.407+2020_407+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_047447359.1:c.407+2020_407+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X8	XM_047447360.1:c.317+2020=	XM_047447360.1:c.317+2019_317+2020dup	XM_047447360.1:c.317+2020_317+2021insTGTG	XM_047447360.1:c.317+2020_317+2021insTGTGTG	XM_047447360.1:c.317+2020_317+2021insTGTGTGTG	XM_047447360.1:c.317+2020_317+2021insTGTGTGTGTG	XM_047447360.1:c.317+2020_317+2021insTGTGTGTGTGTG	XM_047447360.1:c.317+2020_317+2021insTGTGTGTGTGTGTG	XM_047447360.1:c.317+2020_317+2021insTGTGTGTGTGTGTGTG	XM_047447360.1:c.317+2020_317+2021insTGTGTGTGTGTGTGTGTG	XM_047447360.1:c.317+2020_317+2021insTGTGTGTGTGTGTGTGTGTG	XM_047447360.1:c.317+2020_317+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_047447360.1:c.317+2020_317+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_047447360.1:c.317+2020_317+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X9	XM_047447361.1:c.308+2020=	XM_047447361.1:c.308+2019_308+2020dup	XM_047447361.1:c.308+2020_308+2021insTGTG	XM_047447361.1:c.308+2020_308+2021insTGTGTG	XM_047447361.1:c.308+2020_308+2021insTGTGTGTG	XM_047447361.1:c.308+2020_308+2021insTGTGTGTGTG	XM_047447361.1:c.308+2020_308+2021insTGTGTGTGTGTG	XM_047447361.1:c.308+2020_308+2021insTGTGTGTGTGTGTG	XM_047447361.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTG	XM_047447361.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTG	XM_047447361.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTGTG	XM_047447361.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_047447361.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_047447361.1:c.308+2020_308+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X10	XM_047447362.1:c.305+2020=	XM_047447362.1:c.305+2019_305+2020dup	XM_047447362.1:c.305+2020_305+2021insTGTG	XM_047447362.1:c.305+2020_305+2021insTGTGTG	XM_047447362.1:c.305+2020_305+2021insTGTGTGTG	XM_047447362.1:c.305+2020_305+2021insTGTGTGTGTG	XM_047447362.1:c.305+2020_305+2021insTGTGTGTGTGTG	XM_047447362.1:c.305+2020_305+2021insTGTGTGTGTGTGTG	XM_047447362.1:c.305+2020_305+2021insTGTGTGTGTGTGTGTG	XM_047447362.1:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTG	XM_047447362.1:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTGTG	XM_047447362.1:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_047447362.1:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_047447362.1:c.305+2020_305+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X13	XM_047447363.1:c.83+2020=	XM_047447363.1:c.83+2019_83+2020dup	XM_047447363.1:c.83+2020_83+2021insTGTG	XM_047447363.1:c.83+2020_83+2021insTGTGTG	XM_047447363.1:c.83+2020_83+2021insTGTGTGTG	XM_047447363.1:c.83+2020_83+2021insTGTGTGTGTG	XM_047447363.1:c.83+2020_83+2021insTGTGTGTGTGTG	XM_047447363.1:c.83+2020_83+2021insTGTGTGTGTGTGTG	XM_047447363.1:c.83+2020_83+2021insTGTGTGTGTGTGTGTG	XM_047447363.1:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTG	XM_047447363.1:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTG	XM_047447363.1:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_047447363.1:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_047447363.1:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG
ADCY5 transcript variant X14	XM_047447364.1:c.83+2020=	XM_047447364.1:c.83+2019_83+2020dup	XM_047447364.1:c.83+2020_83+2021insTGTG	XM_047447364.1:c.83+2020_83+2021insTGTGTG	XM_047447364.1:c.83+2020_83+2021insTGTGTGTG	XM_047447364.1:c.83+2020_83+2021insTGTGTGTGTG	XM_047447364.1:c.83+2020_83+2021insTGTGTGTGTGTG	XM_047447364.1:c.83+2020_83+2021insTGTGTGTGTGTGTG	XM_047447364.1:c.83+2020_83+2021insTGTGTGTGTGTGTGTG	XM_047447364.1:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTG	XM_047447364.1:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTG	XM_047447364.1:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTGTG	XM_047447364.1:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTGTGTG	XM_047447364.1:c.83+2020_83+2021insTGTGTGTGTGTGTGTGTGTGTGTGTG

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

27 SubSNP, 25 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	KOGIC	ss3952298016	Apr 25, 2020 (154)
2	KOGIC	ss3952298017	Apr 25, 2020 (154)
3	KOGIC	ss3952298018	Apr 25, 2020 (154)
4	GNOMAD	ss4079867937	Apr 26, 2021 (155)
5	GNOMAD	ss4079867938	Apr 26, 2021 (155)
6	GNOMAD	ss4079867939	Apr 26, 2021 (155)
7	GNOMAD	ss4079867940	Apr 26, 2021 (155)
8	GNOMAD	ss4079867941	Apr 26, 2021 (155)
9	GNOMAD	ss4079867942	Apr 26, 2021 (155)
10	GNOMAD	ss4079867943	Apr 26, 2021 (155)
11	GNOMAD	ss4079867944	Apr 26, 2021 (155)
12	GNOMAD	ss4079867945	Apr 26, 2021 (155)
13	GNOMAD	ss4079867946	Apr 26, 2021 (155)
14	GNOMAD	ss4079867947	Apr 26, 2021 (155)
15	GNOMAD	ss4079867948	Apr 26, 2021 (155)
16	GNOMAD	ss4079867949	Apr 26, 2021 (155)
17	TOMMO_GENOMICS	ss5161333343	Apr 26, 2021 (155)
18	TOMMO_GENOMICS	ss5161333344	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5161333345	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5161333346	Apr 26, 2021 (155)
21	1000G_HIGH_COVERAGE	ss5255834092	Oct 12, 2022 (156)
22	HUGCELL_USP	ss5455000592	Oct 12, 2022 (156)
23	HUGCELL_USP	ss5455000593	Oct 12, 2022 (156)
24	TOMMO_GENOMICS	ss5694133001	Oct 12, 2022 (156)
25	TOMMO_GENOMICS	ss5694133002	Oct 12, 2022 (156)
26	TOMMO_GENOMICS	ss5694133003	Oct 12, 2022 (156)
27	TOMMO_GENOMICS	ss5694133004	Oct 12, 2022 (156)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 122220894 (NC_000003.12:123345761::AC 65/32126) Row 122220895 (NC_000003.12:123345761::ACAC 12/32132) Row 122220896 (NC_000003.12:123345761::ACACAC 108/32114)...	-	Apr 26, 2021 (155)
41	Korean Genome Project Submission ignored due to conflicting rows: Row 8676017 (NC_000003.12:123345761::AC 12/1828) Row 8676018 (NC_000003.12:123345761::ACAC 0/1828) Row 8676019 (NC_000003.12:123345761::ACACACAC 2/1828)	-	Apr 25, 2020 (154)
42	Korean Genome Project Submission ignored due to conflicting rows: Row 8676017 (NC_000003.12:123345761::AC 12/1828) Row 8676018 (NC_000003.12:123345761::ACAC 0/1828) Row 8676019 (NC_000003.12:123345761::ACACACAC 2/1828)	-	Apr 25, 2020 (154)
43	Korean Genome Project Submission ignored due to conflicting rows: Row 8676017 (NC_000003.12:123345761::AC 12/1828) Row 8676018 (NC_000003.12:123345761::ACAC 0/1828) Row 8676019 (NC_000003.12:123345761::ACACACAC 2/1828)	-	Apr 25, 2020 (154)
44	8.3KJPN Submission ignored due to conflicting rows: Row 19302650 (NC_000003.11:123064608::ACAC 4/16564) Row 19302651 (NC_000003.11:123064608::AC 62/16564) Row 19302652 (NC_000003.11:123064608::ACACACACAC 1/16564)...	-	Apr 26, 2021 (155)
45	8.3KJPN Submission ignored due to conflicting rows: Row 19302650 (NC_000003.11:123064608::ACAC 4/16564) Row 19302651 (NC_000003.11:123064608::AC 62/16564) Row 19302652 (NC_000003.11:123064608::ACACACACAC 1/16564)...	-	Apr 26, 2021 (155)
46	8.3KJPN Submission ignored due to conflicting rows: Row 19302650 (NC_000003.11:123064608::ACAC 4/16564) Row 19302651 (NC_000003.11:123064608::AC 62/16564) Row 19302652 (NC_000003.11:123064608::ACACACACAC 1/16564)...	-	Apr 26, 2021 (155)
47	8.3KJPN Submission ignored due to conflicting rows: Row 19302650 (NC_000003.11:123064608::ACAC 4/16564) Row 19302651 (NC_000003.11:123064608::AC 62/16564) Row 19302652 (NC_000003.11:123064608::ACACACACAC 1/16564)...	-	Apr 26, 2021 (155)
48	14KJPN Submission ignored due to conflicting rows: Row 27970105 (NC_000003.12:123345761::ACAC 9/27896) Row 27970106 (NC_000003.12:123345761::AC 91/27896) Row 27970107 (NC_000003.12:123345761::ACACACAC 33/27896)...	-	Oct 12, 2022 (156)
49	14KJPN Submission ignored due to conflicting rows: Row 27970105 (NC_000003.12:123345761::ACAC 9/27896) Row 27970106 (NC_000003.12:123345761::AC 91/27896) Row 27970107 (NC_000003.12:123345761::ACACACAC 33/27896)...	-	Oct 12, 2022 (156)
50	14KJPN Submission ignored due to conflicting rows: Row 27970105 (NC_000003.12:123345761::ACAC 9/27896) Row 27970106 (NC_000003.12:123345761::AC 91/27896) Row 27970107 (NC_000003.12:123345761::ACACACAC 33/27896)...	-	Oct 12, 2022 (156)
51	14KJPN Submission ignored due to conflicting rows: Row 27970105 (NC_000003.12:123345761::ACAC 9/27896) Row 27970106 (NC_000003.12:123345761::AC 91/27896) Row 27970107 (NC_000003.12:123345761::ACACACAC 33/27896)...	-	Oct 12, 2022 (156)
52	ALFA	NC_000003.12 - 123345762	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5161333344	NC_000003.11:123064608::AC	NC_000003.12:123345761:ACA:ACACA	(self)
ss3952298016, ss4079867937, ss5455000592, ss5694133002	NC_000003.12:123345761::AC	NC_000003.12:123345761:ACA:ACACA	(self)
13828413796	NC_000003.12:123345761:ACA:ACACA	NC_000003.12:123345761:ACA:ACACA	(self)
ss5161333343	NC_000003.11:123064608::ACAC	NC_000003.12:123345761:ACA:ACACACA	(self)
ss3952298017, ss4079867938, ss5694133001	NC_000003.12:123345761::ACAC	NC_000003.12:123345761:ACA:ACACACA	(self)
13828413796	NC_000003.12:123345761:ACA:ACACACA	NC_000003.12:123345761:ACA:ACACACA	(self)
ss4079867939, ss5455000593	NC_000003.12:123345761::ACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACA	(self)
13828413796	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACA	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACA	(self)
ss5161333346	NC_000003.11:123064608::ACACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACA	(self)
ss3952298018, ss4079867940, ss5694133003	NC_000003.12:123345761::ACACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACA	(self)
13828413796	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACA	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACA	(self)
ss5161333345	NC_000003.11:123064608::ACACACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACA	(self)
ss4079867941, ss5694133004	NC_000003.12:123345761::ACACACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACA	(self)
13828413796	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACA	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACA	(self)
ss4079867942, ss5255834092	NC_000003.12:123345761::ACACACACAC… NC_000003.12:123345761::ACACACACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACA	(self)
13828413796	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACA	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACA	(self)
ss4079867943	NC_000003.12:123345761::ACACACACAC… NC_000003.12:123345761::ACACACACACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACA	(self)
13828413796	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACA	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACA	(self)
ss4079867944	NC_000003.12:123345761::ACACACACAC… NC_000003.12:123345761::ACACACACACACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACACA	(self)
13828413796	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACACA	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACACA	(self)
ss4079867945	NC_000003.12:123345761::ACACACACAC… NC_000003.12:123345761::ACACACACACACACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACACACA	(self)
ss4079867946	NC_000003.12:123345761::ACACACACAC… NC_000003.12:123345761::ACACACACACACACACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACACACACA	(self)
13828413796	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACACACACA	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACACACACA	(self)
ss4079867947	NC_000003.12:123345761::ACACACACAC… NC_000003.12:123345761::ACACACACACACACACACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACACACACACA	(self)
13828413796	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACACACACACA	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACACACACACA	(self)
ss4079867948	NC_000003.12:123345761::ACACACACAC… NC_000003.12:123345761::ACACACACACACACACACACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACACACACACACA	(self)
ss4079867949	NC_000003.12:123345761::ACACACACAC… NC_000003.12:123345761::ACACACACACACACACACACACACAC	NC_000003.12:123345761:ACA:ACACACA… NC_000003.12:123345761:ACA:ACACACACACACACACACACACACACACA	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1491583420

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491583420