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dbSNP Short Genetic Variations

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.

rs1487570997

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr15:50047446 (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
A>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.000004 (1/251072, GnomAD_exome)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ATP8B4 : Missense Variant
Publications
0 citations
Genomic View
See rs on genome
Help

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").

Download
Study Population Group Sample Size Ref Allele Alt Allele
gnomAD - Exomes Global Study-wide 251072 A=0.999996 C=0.000004
gnomAD - Exomes European Sub 135164 A=1.000000 C=0.000000
gnomAD - Exomes Asian Sub 48958 A=0.99998 C=0.00002
gnomAD - Exomes American Sub 34522 A=1.00000 C=0.00000
gnomAD - Exomes African Sub 16230 A=1.00000 C=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10076 A=1.00000 C=0.00000
gnomAD - Exomes Other Sub 6122 A=1.0000 C=0.0000
Help

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 15 NC_000015.10:g.50047446A>C
GRCh37.p13 chr 15 NC_000015.9:g.50339643A>C
Gene: ATP8B4, ATPase phospholipid transporting 8B4 (putative) (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ATP8B4 transcript variant 1 NM_024837.4:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM NP_079113.2:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant 4 NR_073598.2:n.330T>G N/A Non Coding Transcript Variant
ATP8B4 transcript variant 3 NR_073597.2:n.259T>G N/A Non Coding Transcript Variant
ATP8B4 transcript variant 2 NR_073596.2:n.259T>G N/A Non Coding Transcript Variant
ATP8B4 transcript variant X24 XM_011522058.4:c.35+26681…

XM_011522058.4:c.35+26681T>G

N/A Intron Variant
ATP8B4 transcript variant X23 XM_017022594.1:c.35+26681…

XM_017022594.1:c.35+26681T>G

N/A Intron Variant
ATP8B4 transcript variant X14 XM_047433084.1:c.199-8617…

XM_047433084.1:c.199-8617T>G

N/A Intron Variant
ATP8B4 transcript variant X17 XM_047433087.1:c.199-8617…

XM_047433087.1:c.199-8617T>G

N/A Intron Variant
ATP8B4 transcript variant X18 XM_047433088.1:c.88-8617T…

XM_047433088.1:c.88-8617T>G

N/A Intron Variant
ATP8B4 transcript variant X20 XM_047433090.1:c.88-8617T…

XM_047433090.1:c.88-8617T>G

N/A Intron Variant
ATP8B4 transcript variant X30 XM_047433092.1:c.35+26681…

XM_047433092.1:c.35+26681T>G

N/A Intron Variant
ATP8B4 transcript variant X33 XM_047433094.1:c.88-8617T…

XM_047433094.1:c.88-8617T>G

N/A Intron Variant
ATP8B4 transcript variant X34 XM_047433096.1:c.88-8617T…

XM_047433096.1:c.88-8617T>G

N/A Intron Variant
ATP8B4 transcript variant X25 XM_011522059.1:c. N/A Genic Upstream Transcript Variant
ATP8B4 transcript variant X26 XM_011522060.1:c. N/A Genic Upstream Transcript Variant
ATP8B4 transcript variant X27 XM_011522061.1:c. N/A Genic Upstream Transcript Variant
ATP8B4 transcript variant X28 XM_011522062.1:c. N/A Genic Upstream Transcript Variant
ATP8B4 transcript variant X29 XM_011522063.1:c. N/A Genic Upstream Transcript Variant
ATP8B4 transcript variant X38 XM_011522069.2:c. N/A Genic Upstream Transcript Variant
ATP8B4 transcript variant X41 XM_011522070.2:c. N/A Genic Upstream Transcript Variant
ATP8B4 transcript variant X35 XM_024450069.1:c. N/A Genic Upstream Transcript Variant
ATP8B4 transcript variant X36 XM_047433097.1:c. N/A Genic Upstream Transcript Variant
ATP8B4 transcript variant X37 XM_047433098.1:c. N/A Genic Upstream Transcript Variant
ATP8B4 transcript variant X1 XM_011522046.3:c.217T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X1 XP_011520348.1:p.Ser73Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X2 XM_024450065.2:c.217T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X2 XP_024305833.1:p.Ser73Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X3 XM_011522047.3:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X3 XP_011520349.1:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X4 XM_011522053.2:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X3 XP_011520355.1:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X5 XM_011522049.3:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X3 XP_011520351.1:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X6 XM_011522048.2:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X3 XP_011520350.1:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X7 XM_011522052.4:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X3 XP_011520354.1:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X8 XM_047433082.1:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X3 XP_047289038.1:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X9 XM_017022591.2:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X3 XP_016878080.1:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X10 XM_024450066.2:c.217T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X4 XP_024305834.1:p.Ser73Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X11 XM_024450067.2:c.217T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X5 XP_024305835.1:p.Ser73Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X12 XM_047433083.1:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X6 XP_047289039.1:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X13 XM_017022587.3:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X6 XP_016878076.2:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X15 XM_047433085.1:c.217T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X8 XP_047289041.1:p.Ser73Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X16 XM_047433086.1:c.217T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X9 XP_047289042.1:p.Ser73Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X19 XM_047433089.1:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X12 XP_047289045.1:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X21 XM_011522056.4:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X3 XP_011520358.3:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X22 XM_047433091.1:c.217T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X14 XP_047289047.1:p.Ser73Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X31 XM_047433093.1:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X19 XP_047289049.1:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X32 XM_024450068.2:c.217T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X20 XP_024305836.1:p.Ser73Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X39 XM_047433099.1:c.106T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X25 XP_047289055.1:p.Ser36Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X40 XM_047433100.1:c.217T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X26 XP_047289056.1:p.Ser73Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X42 XM_024450070.2:c.217T>G S [TCG] > A [GCG] Coding Sequence Variant
probable phospholipid-transporting ATPase IM isoform X28 XP_024305838.1:p.Ser73Ala S (Ser) > A (Ala) Missense Variant
ATP8B4 transcript variant X43 XR_002957687.2:n.422T>G N/A Non Coding Transcript Variant
Help

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
Help

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 A= C
GRCh38.p14 chr 15 NC_000015.10:g.50047446= NC_000015.10:g.50047446A>C
GRCh37.p13 chr 15 NC_000015.9:g.50339643= NC_000015.9:g.50339643A>C
ATP8B4 transcript variant X7 XM_011522052.4:c.106= XM_011522052.4:c.106T>G
ATP8B4 transcript variant X6 XM_011522052.3:c.106= XM_011522052.3:c.106T>G
ATP8B4 transcript variant X9 XM_011522052.2:c.106= XM_011522052.2:c.106T>G
ATP8B4 transcript variant X8 XM_011522052.1:c.106= XM_011522052.1:c.106T>G
ATP8B4 transcript variant X21 XM_011522056.4:c.106= XM_011522056.4:c.106T>G
ATP8B4 transcript variant X13 XM_011522056.3:c.106= XM_011522056.3:c.106T>G
ATP8B4 transcript variant X1 XM_011522056.2:c.412= XM_011522056.2:c.412T>G
ATP8B4 transcript variant X12 XM_011522056.1:c.106= XM_011522056.1:c.106T>G
ATP8B4 transcript variant 1 NM_024837.4:c.106= NM_024837.4:c.106T>G
ATP8B4 transcript variant 1 NM_024837.3:c.106= NM_024837.3:c.106T>G
ATP8B4 transcript variant X1 XM_011522046.3:c.217= XM_011522046.3:c.217T>G
ATP8B4 transcript variant X1 XM_011522046.2:c.217= XM_011522046.2:c.217T>G
ATP8B4 transcript variant X1 XM_011522046.1:c.217= XM_011522046.1:c.217T>G
ATP8B4 transcript variant X5 XM_011522049.3:c.106= XM_011522049.3:c.106T>G
ATP8B4 transcript variant X5 XM_011522049.2:c.106= XM_011522049.2:c.106T>G
ATP8B4 transcript variant X5 XM_011522049.1:c.106= XM_011522049.1:c.106T>G
ATP8B4 transcript variant X3 XM_011522047.3:c.106= XM_011522047.3:c.106T>G
ATP8B4 transcript variant X3 XM_011522047.2:c.106= XM_011522047.2:c.106T>G
ATP8B4 transcript variant X3 XM_011522047.1:c.106= XM_011522047.1:c.106T>G
ATP8B4 transcript variant X13 XM_017022587.3:c.106= XM_017022587.3:c.106T>G
ATP8B4 transcript variant X22 XM_017022587.2:c.106= XM_017022587.2:c.106T>G
ATP8B4 transcript variant X2 XM_017022587.1:c.412= XM_017022587.1:c.412T>G
ATP8B4 transcript variant X2 XM_024450065.2:c.217= XM_024450065.2:c.217T>G
ATP8B4 transcript variant X2 XM_024450065.1:c.217= XM_024450065.1:c.217T>G
ATP8B4 transcript variant X9 XM_017022591.2:c.106= XM_017022591.2:c.106T>G
ATP8B4 transcript variant X9 XM_017022591.1:c.106= XM_017022591.1:c.106T>G
ATP8B4 transcript variant 4 NR_073598.2:n.330= NR_073598.2:n.330T>G
ATP8B4 transcript variant 4 NR_073598.1:n.267= NR_073598.1:n.267T>G
ATP8B4 transcript variant X10 XM_024450066.2:c.217= XM_024450066.2:c.217T>G
ATP8B4 transcript variant X10 XM_024450066.1:c.217= XM_024450066.1:c.217T>G
ATP8B4 transcript variant X6 XM_011522048.2:c.106= XM_011522048.2:c.106T>G
ATP8B4 transcript variant X4 XM_011522048.1:c.106= XM_011522048.1:c.106T>G
ATP8B4 transcript variant X11 XM_024450067.2:c.217= XM_024450067.2:c.217T>G
ATP8B4 transcript variant X11 XM_024450067.1:c.217= XM_024450067.1:c.217T>G
ATP8B4 transcript variant X4 XM_011522053.2:c.106= XM_011522053.2:c.106T>G
ATP8B4 transcript variant X8 XM_011522053.1:c.106= XM_011522053.1:c.106T>G
ATP8B4 transcript variant 2 NR_073596.2:n.259= NR_073596.2:n.259T>G
ATP8B4 transcript variant 2 NR_073596.1:n.248= NR_073596.1:n.248T>G
ATP8B4 transcript variant 3 NR_073597.2:n.259= NR_073597.2:n.259T>G
ATP8B4 transcript variant 3 NR_073597.1:n.248= NR_073597.1:n.248T>G
ATP8B4 transcript variant X32 XM_024450068.2:c.217= XM_024450068.2:c.217T>G
ATP8B4 transcript variant X23 XM_024450068.1:c.217= XM_024450068.1:c.217T>G
ATP8B4 transcript variant X42 XM_024450070.2:c.217= XM_024450070.2:c.217T>G
ATP8B4 transcript variant X30 XM_024450070.1:c.217= XM_024450070.1:c.217T>G
ATP8B4 transcript variant X43 XR_002957687.2:n.422= XR_002957687.2:n.422T>G
ATP8B4 transcript variant X31 XR_002957687.1:n.562= XR_002957687.1:n.562T>G
ATP8B4 transcript variant X8 XM_047433082.1:c.106= XM_047433082.1:c.106T>G
ATP8B4 transcript variant X15 XM_047433085.1:c.217= XM_047433085.1:c.217T>G
ATP8B4 transcript variant X16 XM_047433086.1:c.217= XM_047433086.1:c.217T>G
ATP8B4 transcript variant X12 XM_047433083.1:c.106= XM_047433083.1:c.106T>G
ATP8B4 transcript variant X39 XM_047433099.1:c.106= XM_047433099.1:c.106T>G
ATP8B4 transcript variant X22 XM_047433091.1:c.217= XM_047433091.1:c.217T>G
ATP8B4 transcript variant X19 XM_047433089.1:c.106= XM_047433089.1:c.106T>G
ATP8B4 transcript variant X31 XM_047433093.1:c.106= XM_047433093.1:c.106T>G
ATP8B4 transcript variant X40 XM_047433100.1:c.217= XM_047433100.1:c.217T>G
probable phospholipid-transporting ATPase IM isoform X3 XP_011520354.1:p.Ser36= XP_011520354.1:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X3 XP_011520358.3:p.Ser36= XP_011520358.3:p.Ser36Ala
probable phospholipid-transporting ATPase IM NP_079113.2:p.Ser36= NP_079113.2:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X1 XP_011520348.1:p.Ser73= XP_011520348.1:p.Ser73Ala
probable phospholipid-transporting ATPase IM isoform X3 XP_011520351.1:p.Ser36= XP_011520351.1:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X3 XP_011520349.1:p.Ser36= XP_011520349.1:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X6 XP_016878076.2:p.Ser36= XP_016878076.2:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X2 XP_024305833.1:p.Ser73= XP_024305833.1:p.Ser73Ala
probable phospholipid-transporting ATPase IM isoform X3 XP_016878080.1:p.Ser36= XP_016878080.1:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X4 XP_024305834.1:p.Ser73= XP_024305834.1:p.Ser73Ala
probable phospholipid-transporting ATPase IM isoform X3 XP_011520350.1:p.Ser36= XP_011520350.1:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X5 XP_024305835.1:p.Ser73= XP_024305835.1:p.Ser73Ala
probable phospholipid-transporting ATPase IM isoform X3 XP_011520355.1:p.Ser36= XP_011520355.1:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X20 XP_024305836.1:p.Ser73= XP_024305836.1:p.Ser73Ala
probable phospholipid-transporting ATPase IM isoform X28 XP_024305838.1:p.Ser73= XP_024305838.1:p.Ser73Ala
probable phospholipid-transporting ATPase IM isoform X3 XP_047289038.1:p.Ser36= XP_047289038.1:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X8 XP_047289041.1:p.Ser73= XP_047289041.1:p.Ser73Ala
probable phospholipid-transporting ATPase IM isoform X9 XP_047289042.1:p.Ser73= XP_047289042.1:p.Ser73Ala
probable phospholipid-transporting ATPase IM isoform X6 XP_047289039.1:p.Ser36= XP_047289039.1:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X25 XP_047289055.1:p.Ser36= XP_047289055.1:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X14 XP_047289047.1:p.Ser73= XP_047289047.1:p.Ser73Ala
probable phospholipid-transporting ATPase IM isoform X12 XP_047289045.1:p.Ser36= XP_047289045.1:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X19 XP_047289049.1:p.Ser36= XP_047289049.1:p.Ser36Ala
probable phospholipid-transporting ATPase IM isoform X26 XP_047289056.1:p.Ser73= XP_047289056.1:p.Ser73Ala
ATP8B4 transcript variant X24 XM_011522058.4:c.35+26681= XM_011522058.4:c.35+26681T>G
ATP8B4 transcript variant X23 XM_017022594.1:c.35+26681= XM_017022594.1:c.35+26681T>G
ATP8B4 transcript variant X14 XM_047433084.1:c.199-8617= XM_047433084.1:c.199-8617T>G
ATP8B4 transcript variant X17 XM_047433087.1:c.199-8617= XM_047433087.1:c.199-8617T>G
ATP8B4 transcript variant X18 XM_047433088.1:c.88-8617= XM_047433088.1:c.88-8617T>G
ATP8B4 transcript variant X20 XM_047433090.1:c.88-8617= XM_047433090.1:c.88-8617T>G
ATP8B4 transcript variant X30 XM_047433092.1:c.35+26681= XM_047433092.1:c.35+26681T>G
ATP8B4 transcript variant X33 XM_047433094.1:c.88-8617= XM_047433094.1:c.88-8617T>G
ATP8B4 transcript variant X34 XM_047433096.1:c.88-8617= XM_047433096.1:c.88-8617T>G
Help

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#.

1 SubSNP, 1 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss2741241973 Nov 08, 2017 (151)
2 gnomAD - Exomes NC_000015.9 - 50339643 Jul 13, 2019 (153)
Help

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
10507505, ss2741241973 NC_000015.9:50339642:A:C NC_000015.10:50047445:A:C (self)
Help

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

No publications for rs1487570997

Help

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.

Software version is: 2.0.1.post820+afb47a3d