Name: rs1491340615
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.

rs1491340615

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:232650561-232650562 (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: insGAGA / insGAGATTGCAGGCATGAG(CCA…
insGAGA / insGAGATTGCAGGCATGAG(CCA)₂TGCCCAGCTGCC / insGAGATTGCAGGCG / insGAGATTGCAGGCGTAAG(CCA)₂TGCCCAGCTGCC / insGAGATTGCAGGCGTGAG(CCA)₂ / insGAGATTGCAGGCGTGAG(CCA)₂TGCCCAGC / insGAGATTGCAGGCGTGAG(CCA)₂TGCCCAGCTGCC / insGAGATTGCAGGCGTGAG(CCA)₂TGCCCAGTTGCC / insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC
Variation Type: Insertion
Frequency: None

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: EFHD1 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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").

None

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 2	NC_000002.12:g.232650561_232650562insGAGA
GRCh38.p14 chr 2	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC
GRCh38.p14 chr 2	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCG
GRCh38.p14 chr 2	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC
GRCh38.p14 chr 2	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCGTGAGCCACCA
GRCh38.p14 chr 2	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCGTGAGCCACCATGCCCAGC
GRCh38.p14 chr 2	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC
GRCh38.p14 chr 2	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC
GRCh38.p14 chr 2	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC
GRCh37.p13 chr 2	NC_000002.11:g.233515271_233515272insGAGA
GRCh37.p13 chr 2	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC
GRCh37.p13 chr 2	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCG
GRCh37.p13 chr 2	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC
GRCh37.p13 chr 2	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCGTGAGCCACCA
GRCh37.p13 chr 2	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCGTGAGCCACCATGCCCAGC
GRCh37.p13 chr 2	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC
GRCh37.p13 chr 2	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC
GRCh37.p13 chr 2	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC
EFHD1 RefSeqGene	NG_051251.1:g.49505_49506insGAGA
EFHD1 RefSeqGene	NG_051251.1:g.49505_49506insGAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC
EFHD1 RefSeqGene	NG_051251.1:g.49505_49506insGAGATTGCAGGCG
EFHD1 RefSeqGene	NG_051251.1:g.49505_49506insGAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC
EFHD1 RefSeqGene	NG_051251.1:g.49505_49506insGAGATTGCAGGCGTGAGCCACCA
EFHD1 RefSeqGene	NG_051251.1:g.49505_49506insGAGATTGCAGGCGTGAGCCACCATGCCCAGC
EFHD1 RefSeqGene	NG_051251.1:g.49505_49506insGAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC
EFHD1 RefSeqGene	NG_051251.1:g.49505_49506insGAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC
EFHD1 RefSeqGene	NG_051251.1:g.49505_49506insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC

Gene: EFHD1, EF-hand domain family member D1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
EFHD1 transcript variant 2	NM_001243252.2:c.15-12241… NM_001243252.2:c.15-12241_15-12240insGAGA	N/A	Intron Variant
EFHD1 transcript variant 3	NM_001308395.2:c.-35+1207… NM_001308395.2:c.-35+12077_-35+12078insGAGA	N/A	Intron Variant
EFHD1 transcript variant 1	NM_025202.4:c.303-12241_3… NM_025202.4:c.303-12241_303-12240insGAGA	N/A	Intron 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	=	insGAGA	insGAGATTGCAGGCATGAG(CCA)₂TGCCCAGCTGCC	insGAGATTGCAGGCG	insGAGATTGCAGGCGTAAG(CCA)₂TGCCCAGCTGCC	insGAGATTGCAGGCGTGAG(CCA)₂	insGAGATTGCAGGCGTGAG(CCA)₂TGCCCAGC	insGAGATTGCAGGCGTGAG(CCA)₂TGCCCAGCTGCC	insGAGATTGCAGGCGTGAG(CCA)₂TGCCCAGTTGCC	insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC
GRCh38.p14 chr 2	NC_000002.12:g.232650561_232650562=	NC_000002.12:g.232650561_232650562insGAGA	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCG	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCGTGAGCCACCA	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCGTGAGCCACCATGCCCAGC	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC	NC_000002.12:g.232650561_232650562insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC
GRCh37.p13 chr 2	NC_000002.11:g.233515271_233515272=	NC_000002.11:g.233515271_233515272insGAGA	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCG	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCGTGAGCCACCA	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCGTGAGCCACCATGCCCAGC	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC	NC_000002.11:g.233515271_233515272insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC
EFHD1 RefSeqGene	NG_051251.1:g.49505_49506=	NG_051251.1:g.49505_49506insGAGA	NG_051251.1:g.49505_49506insGAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC	NG_051251.1:g.49505_49506insGAGATTGCAGGCG	NG_051251.1:g.49505_49506insGAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC	NG_051251.1:g.49505_49506insGAGATTGCAGGCGTGAGCCACCA	NG_051251.1:g.49505_49506insGAGATTGCAGGCGTGAGCCACCATGCCCAGC	NG_051251.1:g.49505_49506insGAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC	NG_051251.1:g.49505_49506insGAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC	NG_051251.1:g.49505_49506insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC
EFHD1 transcript variant 2	NM_001243252.1:c.15-12240=	NM_001243252.1:c.15-12241_15-12240insGAGA	NM_001243252.1:c.15-12241_15-12240insGAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC	NM_001243252.1:c.15-12241_15-12240insGAGATTGCAGGCG	NM_001243252.1:c.15-12241_15-12240insGAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC	NM_001243252.1:c.15-12241_15-12240insGAGATTGCAGGCGTGAGCCACCA	NM_001243252.1:c.15-12241_15-12240insGAGATTGCAGGCGTGAGCCACCATGCCCAGC	NM_001243252.1:c.15-12241_15-12240insGAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC	NM_001243252.1:c.15-12241_15-12240insGAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC	NM_001243252.1:c.15-12241_15-12240insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC
EFHD1 transcript variant 2	NM_001243252.2:c.15-12240=	NM_001243252.2:c.15-12241_15-12240insGAGA	NM_001243252.2:c.15-12241_15-12240insGAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC	NM_001243252.2:c.15-12241_15-12240insGAGATTGCAGGCG	NM_001243252.2:c.15-12241_15-12240insGAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC	NM_001243252.2:c.15-12241_15-12240insGAGATTGCAGGCGTGAGCCACCA	NM_001243252.2:c.15-12241_15-12240insGAGATTGCAGGCGTGAGCCACCATGCCCAGC	NM_001243252.2:c.15-12241_15-12240insGAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC	NM_001243252.2:c.15-12241_15-12240insGAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC	NM_001243252.2:c.15-12241_15-12240insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC
EFHD1 transcript variant 3	NM_001308395.2:c.-35+12078=	NM_001308395.2:c.-35+12077_-35+12078insGAGA	NM_001308395.2:c.-35+12077_-35+12078insGAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC	NM_001308395.2:c.-35+12077_-35+12078insGAGATTGCAGGCG	NM_001308395.2:c.-35+12077_-35+12078insGAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC	NM_001308395.2:c.-35+12077_-35+12078insGAGATTGCAGGCGTGAGCCACCA	NM_001308395.2:c.-35+12077_-35+12078insGAGATTGCAGGCGTGAGCCACCATGCCCAGC	NM_001308395.2:c.-35+12077_-35+12078insGAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC	NM_001308395.2:c.-35+12077_-35+12078insGAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC	NM_001308395.2:c.-35+12077_-35+12078insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC
EFHD1 transcript variant 1	NM_025202.3:c.303-12240=	NM_025202.3:c.303-12241_303-12240insGAGA	NM_025202.3:c.303-12241_303-12240insGAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC	NM_025202.3:c.303-12241_303-12240insGAGATTGCAGGCG	NM_025202.3:c.303-12241_303-12240insGAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC	NM_025202.3:c.303-12241_303-12240insGAGATTGCAGGCGTGAGCCACCA	NM_025202.3:c.303-12241_303-12240insGAGATTGCAGGCGTGAGCCACCATGCCCAGC	NM_025202.3:c.303-12241_303-12240insGAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC	NM_025202.3:c.303-12241_303-12240insGAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC	NM_025202.3:c.303-12241_303-12240insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC
EFHD1 transcript variant 1	NM_025202.4:c.303-12240=	NM_025202.4:c.303-12241_303-12240insGAGA	NM_025202.4:c.303-12241_303-12240insGAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC	NM_025202.4:c.303-12241_303-12240insGAGATTGCAGGCG	NM_025202.4:c.303-12241_303-12240insGAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC	NM_025202.4:c.303-12241_303-12240insGAGATTGCAGGCGTGAGCCACCA	NM_025202.4:c.303-12241_303-12240insGAGATTGCAGGCGTGAGCCACCATGCCCAGC	NM_025202.4:c.303-12241_303-12240insGAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC	NM_025202.4:c.303-12241_303-12240insGAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC	NM_025202.4:c.303-12241_303-12240insGAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC

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#.

28 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	SWEGEN	ss2991544707	Jan 10, 2018 (151)
2	SWEGEN	ss2991544708	Jan 10, 2018 (151)
3	SWEGEN	ss2991544709	Jan 10, 2018 (151)
4	SWEGEN	ss2991544710	Jan 10, 2018 (151)
5	MCHAISSO	ss3064839768	Jan 10, 2018 (151)
6	GNOMAD	ss4063055957	Apr 26, 2021 (155)
7	GNOMAD	ss4063055958	Apr 26, 2021 (155)
8	GNOMAD	ss4063055959	Apr 26, 2021 (155)
9	GNOMAD	ss4063055960	Apr 26, 2021 (155)
10	GNOMAD	ss4063055961	Apr 26, 2021 (155)
11	GNOMAD	ss4063055962	Apr 26, 2021 (155)
12	TOMMO_GENOMICS	ss5157016906	Apr 26, 2021 (155)
13	TOMMO_GENOMICS	ss5157016907	Apr 26, 2021 (155)
14	TOMMO_GENOMICS	ss5157016908	Apr 26, 2021 (155)
15	TOMMO_GENOMICS	ss5157016909	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5157016910	Apr 26, 2021 (155)
17	1000G_HIGH_COVERAGE	ss5252433392	Oct 12, 2022 (156)
18	1000G_HIGH_COVERAGE	ss5252433393	Oct 12, 2022 (156)
19	HUGCELL_USP	ss5452005146	Oct 12, 2022 (156)
20	HUGCELL_USP	ss5452005147	Oct 12, 2022 (156)
21	HUGCELL_USP	ss5452005148	Oct 12, 2022 (156)
22	SANFORD_IMAGENETICS	ss5631181924	Oct 12, 2022 (156)
23	TOMMO_GENOMICS	ss5688056514	Oct 12, 2022 (156)
24	TOMMO_GENOMICS	ss5688056515	Oct 12, 2022 (156)
25	TOMMO_GENOMICS	ss5688056516	Oct 12, 2022 (156)
26	TOMMO_GENOMICS	ss5688056517	Oct 12, 2022 (156)
27	TOMMO_GENOMICS	ss5688056518	Oct 12, 2022 (156)
28	YY_MCH	ss5803320091	Oct 12, 2022 (156)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 94225519 (NC_000002.12:232650561::GAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC 1/66548) Row 94225520 (NC_000002.12:232650561::GAGATTGCAGGCG 26/66452) Row 94225521 (NC_000002.12:232650561::GAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC 1/66548)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 94225519 (NC_000002.12:232650561::GAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC 1/66548) Row 94225520 (NC_000002.12:232650561::GAGATTGCAGGCG 26/66452) Row 94225521 (NC_000002.12:232650561::GAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC 1/66548)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 94225519 (NC_000002.12:232650561::GAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC 1/66548) Row 94225520 (NC_000002.12:232650561::GAGATTGCAGGCG 26/66452) Row 94225521 (NC_000002.12:232650561::GAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC 1/66548)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 94225519 (NC_000002.12:232650561::GAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC 1/66548) Row 94225520 (NC_000002.12:232650561::GAGATTGCAGGCG 26/66452) Row 94225521 (NC_000002.12:232650561::GAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC 1/66548)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 94225519 (NC_000002.12:232650561::GAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC 1/66548) Row 94225520 (NC_000002.12:232650561::GAGATTGCAGGCG 26/66452) Row 94225521 (NC_000002.12:232650561::GAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC 1/66548)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 94225519 (NC_000002.12:232650561::GAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC 1/66548) Row 94225520 (NC_000002.12:232650561::GAGATTGCAGGCG 26/66452) Row 94225521 (NC_000002.12:232650561::GAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC 1/66548)...	-	Apr 26, 2021 (155)
35	8.3KJPN Submission ignored due to conflicting rows: Row 14986213 (NC_000002.11:233515271::GAGATTGCAGGCG 37/13178) Row 14986214 (NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC 2561/13178) Row 14986215 (NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCATGCCCAGC 102/13178)...	-	Apr 26, 2021 (155)
36	8.3KJPN Submission ignored due to conflicting rows: Row 14986213 (NC_000002.11:233515271::GAGATTGCAGGCG 37/13178) Row 14986214 (NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC 2561/13178) Row 14986215 (NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCATGCCCAGC 102/13178)...	-	Apr 26, 2021 (155)
37	8.3KJPN Submission ignored due to conflicting rows: Row 14986213 (NC_000002.11:233515271::GAGATTGCAGGCG 37/13178) Row 14986214 (NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC 2561/13178) Row 14986215 (NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCATGCCCAGC 102/13178)...	-	Apr 26, 2021 (155)
38	8.3KJPN Submission ignored due to conflicting rows: Row 14986213 (NC_000002.11:233515271::GAGATTGCAGGCG 37/13178) Row 14986214 (NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC 2561/13178) Row 14986215 (NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCATGCCCAGC 102/13178)...	-	Apr 26, 2021 (155)
39	8.3KJPN Submission ignored due to conflicting rows: Row 14986213 (NC_000002.11:233515271::GAGATTGCAGGCG 37/13178) Row 14986214 (NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC 2561/13178) Row 14986215 (NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCATGCCCAGC 102/13178)...	-	Apr 26, 2021 (155)
40	14KJPN Submission ignored due to conflicting rows: Row 21893618 (NC_000002.12:232650561::GAGA 606/21564) Row 21893619 (NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCA 133/21564) Row 21893620 (NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGC 222/21564)...	-	Oct 12, 2022 (156)
41	14KJPN Submission ignored due to conflicting rows: Row 21893618 (NC_000002.12:232650561::GAGA 606/21564) Row 21893619 (NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCA 133/21564) Row 21893620 (NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGC 222/21564)...	-	Oct 12, 2022 (156)
42	14KJPN Submission ignored due to conflicting rows: Row 21893618 (NC_000002.12:232650561::GAGA 606/21564) Row 21893619 (NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCA 133/21564) Row 21893620 (NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGC 222/21564)...	-	Oct 12, 2022 (156)
43	14KJPN Submission ignored due to conflicting rows: Row 21893618 (NC_000002.12:232650561::GAGA 606/21564) Row 21893619 (NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCA 133/21564) Row 21893620 (NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGC 222/21564)...	-	Oct 12, 2022 (156)
44	14KJPN Submission ignored due to conflicting rows: Row 21893618 (NC_000002.12:232650561::GAGA 606/21564) Row 21893619 (NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCA 133/21564) Row 21893620 (NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGC 222/21564)...	-	Oct 12, 2022 (156)

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
ss2991544708, ss5157016910	NC_000002.11:233515271::GAGA	NC_000002.12:232650561::GAGA	(self)
ss5452005148, ss5688056514, ss5803320091	NC_000002.12:232650561::GAGA	NC_000002.12:232650561::GAGA
ss4063055957	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCATGAGCCACCATGCCCAGCTGCC	(self)
ss5157016906	NC_000002.11:233515271::GAGATTGCAG… NC_000002.11:233515271::GAGATTGCAGGCG	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCG	(self)
ss4063055958, ss5688056517	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCG	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCG	(self)
ss4063055959	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTAAGCCACCATGCCCAGCTGCC	(self)
ss2991544710, ss5157016909	NC_000002.11:233515271::GAGATTGCAG… NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCA	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCA	(self)
ss4063055960, ss5252433392, ss5688056515	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCA	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCA	(self)
ss2991544709, ss5157016908	NC_000002.11:233515271::GAGATTGCAG… NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCATGCCCAGC	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGC	(self)
ss5252433393, ss5452005147, ss5688056516	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGC	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGC
ss2991544707, ss5157016907, ss5631181924	NC_000002.11:233515271::GAGATTGCAG… NC_000002.11:233515271::GAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC	(self)
ss3064839768, ss5452005146, ss5688056518	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGCTGCC	(self)
ss4063055961	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCATGCCCAGTTGCC	(self)
ss4063055962	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC	NC_000002.12:232650561::GAGATTGCAG… NC_000002.12:232650561::GAGATTGCAGGCGTGAGCCACCTTGCCCAGCTGCC	(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 rs1491340615

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
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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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491340615