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.
rs1482476318
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr16:57152493 (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
- T>C
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
- C=0.000007 (1/140254, GnomAD)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
- PSME3IP1 : 3 Prime UTR 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").
Download| Study | Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|---|
| gnomAD - Genomes | Global | Study-wide | 140254 | T=0.999993 | C=0.000007 |
| gnomAD - Genomes | European | Sub | 75960 | T=0.99999 | C=0.00001 |
| gnomAD - Genomes | African | Sub | 42038 | T=1.00000 | C=0.00000 |
| gnomAD - Genomes | American | Sub | 13654 | T=1.00000 | C=0.00000 |
| gnomAD - Genomes | Ashkenazi Jewish | Sub | 3320 | T=1.0000 | C=0.0000 |
| gnomAD - Genomes | East Asian | Sub | 3134 | T=1.0000 | C=0.0000 |
| gnomAD - Genomes | Other | Sub | 2148 | T=1.0000 | C=0.0000 |
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.
| Sequence name | Change |
|---|---|
| GRCh38.p14 chr 16 | NC_000016.10:g.57152493T>C |
| GRCh37.p13 chr 16 | NC_000016.9:g.57186405T>C |
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| PSME3IP1 transcript variant 3 | NM_001354080.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 5 | NM_001354082.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 2 | NM_001354079.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 1 | NM_001354078.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 10 | NM_001354087.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 20 | NM_024946.4:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 8 | NM_001354085.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 22 | NM_001354098.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 13 | NM_001354090.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 27 | NM_001354103.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 17 | NM_001354094.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 24 | NM_001354100.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 19 | NM_001354096.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 12 | NM_001354089.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 4 | NM_001354081.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 7 | NM_001354084.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 9 | NM_001354086.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 6 | NM_001354083.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 26 | NM_001354102.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 18 | NM_001354095.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 25 | NM_001354101.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 23 | NM_001354099.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 15 | NM_001354092.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 11 | NM_001354088.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 14 | NM_001354091.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant 21 | NM_001354097.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X17 | XM_017023704.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X1 | XM_047434668.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X2 | XM_047434669.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X3 | XM_047434670.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X4 | XM_047434671.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X5 | XM_047434672.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X6 | XM_047434673.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X7 | XM_047434675.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X8 | XM_047434676.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X9 | XM_017023681.3:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X10 | XM_047434677.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X11 | XM_047434678.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X12 | XM_024450454.2:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X13 | XM_047434679.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X14 | XM_047434680.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X15 | XM_047434681.1:c.*1797= | N/A | 3 Prime UTR Variant |
| PSME3IP1 transcript variant X16 | XM_017023703.2:c.*1797= | N/A | 3 Prime UTR 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.
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 | T= | C |
|---|---|---|
| GRCh38.p14 chr 16 | NC_000016.10:g.57152493= | NC_000016.10:g.57152493T>C |
| GRCh37.p13 chr 16 | NC_000016.9:g.57186405= | NC_000016.9:g.57186405T>C |
| PSME3IP1 transcript variant 20 | NM_024946.4:c.*1797= | NM_024946.4:c.*1797A>G |
| FAM192A transcript variant 20 | NM_024946.3:c.*1797= | NM_024946.3:c.*1797A>G |
| FAM192A transcript | NM_024946.2:c.*1797= | NM_024946.2:c.*1797A>G |
| PSME3IP1 transcript variant X9 | XM_017023681.3:c.*1797= | XM_017023681.3:c.*1797A>G |
| PSME3IP1 transcript variant X3 | XM_017023681.2:c.*1797= | XM_017023681.2:c.*1797A>G |
| FAM192A transcript variant X4 | XM_017023681.1:c.*1797= | XM_017023681.1:c.*1797A>G |
| PSME3IP1 transcript variant 27 | NM_001354103.2:c.*1797= | NM_001354103.2:c.*1797A>G |
| FAM192A transcript variant 27 | NM_001354103.1:c.*1797= | NM_001354103.1:c.*1797A>G |
| PSME3IP1 transcript variant 26 | NM_001354102.2:c.*1797= | NM_001354102.2:c.*1797A>G |
| FAM192A transcript variant 26 | NM_001354102.1:c.*1797= | NM_001354102.1:c.*1797A>G |
| PSME3IP1 transcript variant 25 | NM_001354101.2:c.*1797= | NM_001354101.2:c.*1797A>G |
| FAM192A transcript variant 25 | NM_001354101.1:c.*1797= | NM_001354101.1:c.*1797A>G |
| PSME3IP1 transcript variant 23 | NM_001354099.2:c.*1797= | NM_001354099.2:c.*1797A>G |
| FAM192A transcript variant 23 | NM_001354099.1:c.*1797= | NM_001354099.1:c.*1797A>G |
| PSME3IP1 transcript variant 24 | NM_001354100.2:c.*1797= | NM_001354100.2:c.*1797A>G |
| FAM192A transcript variant 24 | NM_001354100.1:c.*1797= | NM_001354100.1:c.*1797A>G |
| PSME3IP1 transcript variant 22 | NM_001354098.2:c.*1797= | NM_001354098.2:c.*1797A>G |
| FAM192A transcript variant 22 | NM_001354098.1:c.*1797= | NM_001354098.1:c.*1797A>G |
| PSME3IP1 transcript variant 19 | NM_001354096.2:c.*1797= | NM_001354096.2:c.*1797A>G |
| FAM192A transcript variant 19 | NM_001354096.1:c.*1797= | NM_001354096.1:c.*1797A>G |
| PSME3IP1 transcript variant 15 | NM_001354092.2:c.*1797= | NM_001354092.2:c.*1797A>G |
| FAM192A transcript variant 15 | NM_001354092.1:c.*1797= | NM_001354092.1:c.*1797A>G |
| PSME3IP1 transcript variant 13 | NM_001354090.2:c.*1797= | NM_001354090.2:c.*1797A>G |
| FAM192A transcript variant 13 | NM_001354090.1:c.*1797= | NM_001354090.1:c.*1797A>G |
| PSME3IP1 transcript variant 8 | NM_001354085.2:c.*1797= | NM_001354085.2:c.*1797A>G |
| FAM192A transcript variant 8 | NM_001354085.1:c.*1797= | NM_001354085.1:c.*1797A>G |
| PSME3IP1 transcript variant 11 | NM_001354088.2:c.*1797= | NM_001354088.2:c.*1797A>G |
| FAM192A transcript variant 11 | NM_001354088.1:c.*1797= | NM_001354088.1:c.*1797A>G |
| PSME3IP1 transcript variant 7 | NM_001354084.2:c.*1797= | NM_001354084.2:c.*1797A>G |
| FAM192A transcript variant 7 | NM_001354084.1:c.*1797= | NM_001354084.1:c.*1797A>G |
| PSME3IP1 transcript variant 12 | NM_001354089.2:c.*1797= | NM_001354089.2:c.*1797A>G |
| FAM192A transcript variant 12 | NM_001354089.1:c.*1797= | NM_001354089.1:c.*1797A>G |
| PSME3IP1 transcript variant 14 | NM_001354091.2:c.*1797= | NM_001354091.2:c.*1797A>G |
| FAM192A transcript variant 14 | NM_001354091.1:c.*1797= | NM_001354091.1:c.*1797A>G |
| PSME3IP1 transcript variant 18 | NM_001354095.2:c.*1797= | NM_001354095.2:c.*1797A>G |
| FAM192A transcript variant 18 | NM_001354095.1:c.*1797= | NM_001354095.1:c.*1797A>G |
| PSME3IP1 transcript variant 17 | NM_001354094.2:c.*1797= | NM_001354094.2:c.*1797A>G |
| FAM192A transcript variant 17 | NM_001354094.1:c.*1797= | NM_001354094.1:c.*1797A>G |
| PSME3IP1 transcript variant 4 | NM_001354081.2:c.*1797= | NM_001354081.2:c.*1797A>G |
| FAM192A transcript variant 4 | NM_001354081.1:c.*1797= | NM_001354081.1:c.*1797A>G |
| PSME3IP1 transcript variant 21 | NM_001354097.2:c.*1797= | NM_001354097.2:c.*1797A>G |
| FAM192A transcript variant 21 | NM_001354097.1:c.*1797= | NM_001354097.1:c.*1797A>G |
| PSME3IP1 transcript variant 9 | NM_001354086.2:c.*1797= | NM_001354086.2:c.*1797A>G |
| FAM192A transcript variant 9 | NM_001354086.1:c.*1797= | NM_001354086.1:c.*1797A>G |
| PSME3IP1 transcript variant X12 | XM_024450454.2:c.*1797= | XM_024450454.2:c.*1797A>G |
| PSME3IP1 transcript variant X9 | XM_024450454.1:c.*1797= | XM_024450454.1:c.*1797A>G |
| PSME3IP1 transcript variant 6 | NM_001354083.2:c.*1797= | NM_001354083.2:c.*1797A>G |
| FAM192A transcript variant 6 | NM_001354083.1:c.*1797= | NM_001354083.1:c.*1797A>G |
| PSME3IP1 transcript variant X16 | XM_017023703.2:c.*1797= | XM_017023703.2:c.*1797A>G |
| PSME3IP1 transcript variant X10 | XM_017023703.1:c.*1797= | XM_017023703.1:c.*1797A>G |
| PSME3IP1 transcript variant X6 | XM_047434673.1:c.*1797= | XM_047434673.1:c.*1797A>G |
| PSME3IP1 transcript variant X3 | XM_047434670.1:c.*1797= | XM_047434670.1:c.*1797A>G |
| PSME3IP1 transcript variant X7 | XM_047434675.1:c.*1797= | XM_047434675.1:c.*1797A>G |
| PSME3IP1 transcript variant X4 | XM_047434671.1:c.*1797= | XM_047434671.1:c.*1797A>G |
| PSME3IP1 transcript variant X5 | XM_047434672.1:c.*1797= | XM_047434672.1:c.*1797A>G |
| PSME3IP1 transcript variant X10 | XM_047434677.1:c.*1797= | XM_047434677.1:c.*1797A>G |
| PSME3IP1 transcript variant X2 | XM_047434669.1:c.*1797= | XM_047434669.1:c.*1797A>G |
| PSME3IP1 transcript variant 10 | NM_001354087.1:c.*1797= | NM_001354087.1:c.*1797A>G |
| PSME3IP1 transcript variant 2 | NM_001354079.1:c.*1797= | NM_001354079.1:c.*1797A>G |
| PSME3IP1 transcript variant 3 | NM_001354080.1:c.*1797= | NM_001354080.1:c.*1797A>G |
| PSME3IP1 transcript variant X8 | XM_047434676.1:c.*1797= | XM_047434676.1:c.*1797A>G |
| PSME3IP1 transcript variant X11 | XM_047434678.1:c.*1797= | XM_047434678.1:c.*1797A>G |
| FAM192A transcript variant 16 | NM_001354093.1:c.*1797= | NM_001354093.1:c.*1797A>G |
| PSME3IP1 transcript variant X13 | XM_047434679.1:c.*1797= | XM_047434679.1:c.*1797A>G |
| PSME3IP1 transcript variant X14 | XM_047434680.1:c.*1797= | XM_047434680.1:c.*1797A>G |
| PSME3IP1 transcript variant X15 | XM_047434681.1:c.*1797= | XM_047434681.1:c.*1797A>G |
| PSME3IP1 transcript variant X1 | XM_047434668.1:c.*1797= | XM_047434668.1:c.*1797A>G |
| PSME3IP1 transcript variant 5 | NM_001354082.1:c.*1797= | NM_001354082.1:c.*1797A>G |
| PSME3IP1 transcript variant 1 | NM_001354078.1:c.*1797= | NM_001354078.1:c.*1797A>G |
| PSME3IP1 transcript variant X17 | XM_017023704.1:c.*1797= | XM_017023704.1:c.*1797A>G |
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#.
| No | Submitter | Submission ID | Date (Build) |
|---|---|---|---|
| 1 | GNOMAD | ss2943429787 | Nov 08, 2017 (151) |
| 2 | gnomAD - Genomes | NC_000016.10 - 57152493 | Apr 27, 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).
Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
No publications for rs1482476318
The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.
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.
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.