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.
rs1481164883
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr3:188609393 (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=0.000004 (1/251120, GnomAD_exome)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
-
LPP : Missense VariantLOC124906316 : Intron 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 | 251120 | T=0.999996 | C=0.000004 |
| gnomAD - Exomes | European | Sub | 135108 | T=0.999993 | C=0.000007 |
| gnomAD - Exomes | Asian | Sub | 48988 | T=1.00000 | C=0.00000 |
| gnomAD - Exomes | American | Sub | 34578 | T=1.00000 | C=0.00000 |
| gnomAD - Exomes | African | Sub | 16254 | T=1.00000 | C=0.00000 |
| gnomAD - Exomes | Ashkenazi Jewish | Sub | 10062 | T=1.00000 | C=0.00000 |
| gnomAD - Exomes | Other | Sub | 6130 | T=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 3 | NC_000003.12:g.188609393T>C |
| GRCh37.p13 chr 3 | NC_000003.11:g.188327181T>C |
| LPP RefSeqGene | NG_016932.2:g.460519T>C |
Gene: LPP, LIM domain containing preferred translocation partner in lipoma
(plus strand)
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| LPP transcript variant 3 | NM_001167672.3:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform b | NP_001161144.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 11 | NM_001375462.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001362391.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 12 | NM_001375463.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001362392.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 13 | NM_001375465.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001362394.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 1 | NM_005578.5:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_005569.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 9 | NM_001375459.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001362388.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 7 | NM_001375461.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001362390.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 14 | NM_001375464.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001362393.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 8 | NM_001375458.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001362387.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 2 | NM_001167671.3:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001161143.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 10 | NM_001375460.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001362389.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 4 | NM_001375455.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001362384.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 5 | NM_001375456.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001362385.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 6 | NM_001375457.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001362386.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 34 | NM_001387681.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform d | NP_001374610.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 30 | NM_001387677.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform d | NP_001374606.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 35 | NM_001387682.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform d | NP_001374611.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 33 | NM_001387680.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform d | NP_001374609.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 31 | NM_001387678.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform d | NP_001374607.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 36 | NM_001387683.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform d | NP_001374612.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 32 | NM_001387679.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform d | NP_001374608.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 16 | NM_001387663.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001374592.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 17 | NM_001387664.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001374593.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 20 | NM_001387667.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001374596.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 19 | NM_001387666.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001374595.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 18 | NM_001387665.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001374594.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 28 | NM_001387675.1:c.173T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform c | NP_001374604.1:p.Phe58Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 29 | NM_001387676.1:c.173T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform c | NP_001374605.1:p.Phe58Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 26 | NM_001387673.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001374602.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 23 | NM_001387670.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001374599.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 21 | NM_001387668.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001374597.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 22 | NM_001387669.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001374598.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 25 | NM_001387672.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001374601.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 27 | NM_001387674.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001374603.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 24 | NM_001387671.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform a | NP_001374600.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant 15 | NR_164692.1:n.918T>C | N/A | Non Coding Transcript Variant |
| LPP transcript variant X23 | XM_017006381.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X8 | XP_016861870.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X1 | XM_047448097.1:c.854T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X1 | XP_047304053.1:p.Phe285Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X2 | XM_047448098.1:c.797T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X2 | XP_047304054.1:p.Phe266Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X3 | XM_011512823.3:c.737T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X3 | XP_011511125.1:p.Phe246Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X4 | XM_047448099.1:c.731T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X4 | XP_047304055.1:p.Phe244Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X5 | XM_047448100.1:c.722T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X5 | XP_047304056.1:p.Phe241Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X6 | XM_047448101.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304057.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X7 | XM_047448102.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304058.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X8 | XM_047448103.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304059.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X9 | XM_047448104.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304060.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X10 | XM_047448105.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304061.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X11 | XM_047448106.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304062.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X12 | XM_047448107.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304063.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X13 | XM_047448108.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304064.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X14 | XM_047448109.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304065.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X15 | XM_047448110.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304066.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X16 | XM_047448111.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304067.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X17 | XM_047448112.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304068.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X18 | XM_047448113.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304069.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X19 | XM_047448114.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304070.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X20 | XM_047448115.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_047304071.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X21 | XM_047448116.1:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X7 | XP_047304072.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
| LPP transcript variant X22 | XM_017006378.2:c.662T>C | F [TTT] > S [TCT] | Coding Sequence Variant |
| lipoma-preferred partner isoform X6 | XP_016861867.1:p.Phe221Ser | F (Phe) > S (Ser) | Missense Variant |
Gene: LOC124906316, uncharacterized LOC124906316
(minus strand)
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| LOC124906316 transcript | XR_007096213.1:n. | N/A | Intron 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 | T= | C |
|---|---|---|
| GRCh38.p14 chr 3 | NC_000003.12:g.188609393= | NC_000003.12:g.188609393T>C |
| GRCh37.p13 chr 3 | NC_000003.11:g.188327181= | NC_000003.11:g.188327181T>C |
| LPP RefSeqGene | NG_016932.2:g.460519= | NG_016932.2:g.460519T>C |
| LPP transcript variant 1 | NM_005578.5:c.662= | NM_005578.5:c.662T>C |
| LPP transcript variant 1 | NM_005578.4:c.662= | NM_005578.4:c.662T>C |
| LPP transcript variant 1 | NM_005578.3:c.662= | NM_005578.3:c.662T>C |
| LPP transcript variant 2 | NM_001167671.3:c.662= | NM_001167671.3:c.662T>C |
| LPP transcript variant 2 | NM_001167671.2:c.662= | NM_001167671.2:c.662T>C |
| LPP transcript variant 2 | NM_001167671.1:c.662= | NM_001167671.1:c.662T>C |
| LPP transcript variant 3 | NM_001167672.3:c.662= | NM_001167672.3:c.662T>C |
| LPP transcript variant 3 | NM_001167672.2:c.662= | NM_001167672.2:c.662T>C |
| LPP transcript variant 3 | NM_001167672.1:c.662= | NM_001167672.1:c.662T>C |
| LPP transcript variant 6 | NM_001375457.1:c.662= | NM_001375457.1:c.662T>C |
| LPP transcript variant 20 | NM_001387667.1:c.662= | NM_001387667.1:c.662T>C |
| LPP transcript variant 4 | NM_001375455.1:c.662= | NM_001375455.1:c.662T>C |
| LPP transcript variant 5 | NM_001375456.1:c.662= | NM_001375456.1:c.662T>C |
| LPP transcript variant 18 | NM_001387665.1:c.662= | NM_001387665.1:c.662T>C |
| LPP transcript variant 27 | NM_001387674.1:c.662= | NM_001387674.1:c.662T>C |
| LPP transcript variant 10 | NM_001375460.1:c.662= | NM_001375460.1:c.662T>C |
| LPP transcript variant 25 | NM_001387672.1:c.662= | NM_001387672.1:c.662T>C |
| LPP transcript variant 7 | NM_001375461.1:c.662= | NM_001375461.1:c.662T>C |
| LPP transcript variant 17 | NM_001387664.1:c.662= | NM_001387664.1:c.662T>C |
| LPP transcript variant 19 | NM_001387666.1:c.662= | NM_001387666.1:c.662T>C |
| LPP transcript variant 8 | NM_001375458.1:c.662= | NM_001375458.1:c.662T>C |
| LPP transcript variant 24 | NM_001387671.1:c.662= | NM_001387671.1:c.662T>C |
| LPP transcript variant 22 | NM_001387669.1:c.662= | NM_001387669.1:c.662T>C |
| LPP transcript variant 14 | NM_001375464.1:c.662= | NM_001375464.1:c.662T>C |
| LPP transcript variant 11 | NM_001375462.1:c.662= | NM_001375462.1:c.662T>C |
| LPP transcript variant 9 | NM_001375459.1:c.662= | NM_001375459.1:c.662T>C |
| LPP transcript variant 12 | NM_001375463.1:c.662= | NM_001375463.1:c.662T>C |
| LPP transcript variant 26 | NM_001387673.1:c.662= | NM_001387673.1:c.662T>C |
| LPP transcript variant 15 | NR_164692.1:n.918= | NR_164692.1:n.918T>C |
| LPP transcript variant 13 | NM_001375465.1:c.662= | NM_001375465.1:c.662T>C |
| LPP transcript variant 21 | NM_001387668.1:c.662= | NM_001387668.1:c.662T>C |
| LPP transcript variant 16 | NM_001387663.1:c.662= | NM_001387663.1:c.662T>C |
| LPP transcript variant 23 | NM_001387670.1:c.662= | NM_001387670.1:c.662T>C |
| LPP transcript variant 28 | NM_001387675.1:c.173= | NM_001387675.1:c.173T>C |
| LPP transcript variant 29 | NM_001387676.1:c.173= | NM_001387676.1:c.173T>C |
| LPP transcript variant 31 | NM_001387678.1:c.662= | NM_001387678.1:c.662T>C |
| LPP transcript variant 35 | NM_001387682.1:c.662= | NM_001387682.1:c.662T>C |
| LPP transcript variant 34 | NM_001387681.1:c.662= | NM_001387681.1:c.662T>C |
| LPP transcript variant 33 | NM_001387680.1:c.662= | NM_001387680.1:c.662T>C |
| LPP transcript variant 30 | NM_001387677.1:c.662= | NM_001387677.1:c.662T>C |
| LPP transcript variant 36 | NM_001387683.1:c.662= | NM_001387683.1:c.662T>C |
| LPP transcript variant 32 | NM_001387679.1:c.662= | NM_001387679.1:c.662T>C |
| LPP transcript variant X3 | XM_011512823.3:c.737= | XM_011512823.3:c.737T>C |
| LPP transcript variant X1 | XM_011512823.2:c.737= | XM_011512823.2:c.737T>C |
| LPP transcript variant X4 | XM_011512823.1:c.737= | XM_011512823.1:c.737T>C |
| LPP transcript variant X22 | XM_017006378.2:c.662= | XM_017006378.2:c.662T>C |
| LPP transcript variant X7 | XM_017006378.1:c.662= | XM_017006378.1:c.662T>C |
| LPP transcript variant X5 | XM_047448100.1:c.722= | XM_047448100.1:c.722T>C |
| LPP transcript variant X8 | XM_047448103.1:c.662= | XM_047448103.1:c.662T>C |
| LPP transcript variant X20 | XM_047448115.1:c.662= | XM_047448115.1:c.662T>C |
| LPP transcript variant X10 | XM_047448105.1:c.662= | XM_047448105.1:c.662T>C |
| LPP transcript variant X14 | XM_047448109.1:c.662= | XM_047448109.1:c.662T>C |
| LPP transcript variant X7 | XM_047448102.1:c.662= | XM_047448102.1:c.662T>C |
| LPP transcript variant X6 | XM_047448101.1:c.662= | XM_047448101.1:c.662T>C |
| LPP transcript variant X9 | XM_047448104.1:c.662= | XM_047448104.1:c.662T>C |
| LPP transcript variant X13 | XM_047448108.1:c.662= | XM_047448108.1:c.662T>C |
| LPP transcript variant X11 | XM_047448106.1:c.662= | XM_047448106.1:c.662T>C |
| LPP transcript variant X1 | XM_047448097.1:c.854= | XM_047448097.1:c.854T>C |
| LPP transcript variant X19 | XM_047448114.1:c.662= | XM_047448114.1:c.662T>C |
| LPP transcript variant X15 | XM_047448110.1:c.662= | XM_047448110.1:c.662T>C |
| LPP transcript variant X18 | XM_047448113.1:c.662= | XM_047448113.1:c.662T>C |
| LPP transcript variant X17 | XM_047448112.1:c.662= | XM_047448112.1:c.662T>C |
| LPP transcript variant X16 | XM_047448111.1:c.662= | XM_047448111.1:c.662T>C |
| LPP transcript variant X4 | XM_047448099.1:c.731= | XM_047448099.1:c.731T>C |
| LPP transcript variant X12 | XM_047448107.1:c.662= | XM_047448107.1:c.662T>C |
| LPP transcript variant X2 | XM_047448098.1:c.797= | XM_047448098.1:c.797T>C |
| LPP transcript variant X21 | XM_047448116.1:c.662= | XM_047448116.1:c.662T>C |
| LPP transcript variant X23 | XM_017006381.1:c.662= | XM_017006381.1:c.662T>C |
| lipoma-preferred partner isoform a | NP_005569.1:p.Phe221= | NP_005569.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001161143.1:p.Phe221= | NP_001161143.1:p.Phe221Ser |
| lipoma-preferred partner isoform b | NP_001161144.1:p.Phe221= | NP_001161144.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001362386.1:p.Phe221= | NP_001362386.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001374596.1:p.Phe221= | NP_001374596.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001362384.1:p.Phe221= | NP_001362384.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001362385.1:p.Phe221= | NP_001362385.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001374594.1:p.Phe221= | NP_001374594.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001374603.1:p.Phe221= | NP_001374603.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001362389.1:p.Phe221= | NP_001362389.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001374601.1:p.Phe221= | NP_001374601.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001362390.1:p.Phe221= | NP_001362390.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001374593.1:p.Phe221= | NP_001374593.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001374595.1:p.Phe221= | NP_001374595.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001362387.1:p.Phe221= | NP_001362387.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001374600.1:p.Phe221= | NP_001374600.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001374598.1:p.Phe221= | NP_001374598.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001362393.1:p.Phe221= | NP_001362393.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001362391.1:p.Phe221= | NP_001362391.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001362388.1:p.Phe221= | NP_001362388.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001362392.1:p.Phe221= | NP_001362392.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001374602.1:p.Phe221= | NP_001374602.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001362394.1:p.Phe221= | NP_001362394.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001374597.1:p.Phe221= | NP_001374597.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001374592.1:p.Phe221= | NP_001374592.1:p.Phe221Ser |
| lipoma-preferred partner isoform a | NP_001374599.1:p.Phe221= | NP_001374599.1:p.Phe221Ser |
| lipoma-preferred partner isoform c | NP_001374604.1:p.Phe58= | NP_001374604.1:p.Phe58Ser |
| lipoma-preferred partner isoform c | NP_001374605.1:p.Phe58= | NP_001374605.1:p.Phe58Ser |
| lipoma-preferred partner isoform d | NP_001374607.1:p.Phe221= | NP_001374607.1:p.Phe221Ser |
| lipoma-preferred partner isoform d | NP_001374611.1:p.Phe221= | NP_001374611.1:p.Phe221Ser |
| lipoma-preferred partner isoform d | NP_001374610.1:p.Phe221= | NP_001374610.1:p.Phe221Ser |
| lipoma-preferred partner isoform d | NP_001374609.1:p.Phe221= | NP_001374609.1:p.Phe221Ser |
| lipoma-preferred partner isoform d | NP_001374606.1:p.Phe221= | NP_001374606.1:p.Phe221Ser |
| lipoma-preferred partner isoform d | NP_001374612.1:p.Phe221= | NP_001374612.1:p.Phe221Ser |
| lipoma-preferred partner isoform d | NP_001374608.1:p.Phe221= | NP_001374608.1:p.Phe221Ser |
| lipoma-preferred partner isoform X3 | XP_011511125.1:p.Phe246= | XP_011511125.1:p.Phe246Ser |
| lipoma-preferred partner isoform X6 | XP_016861867.1:p.Phe221= | XP_016861867.1:p.Phe221Ser |
| lipoma-preferred partner isoform X5 | XP_047304056.1:p.Phe241= | XP_047304056.1:p.Phe241Ser |
| lipoma-preferred partner isoform X6 | XP_047304059.1:p.Phe221= | XP_047304059.1:p.Phe221Ser |
| lipoma-preferred partner isoform X6 | XP_047304071.1:p.Phe221= | XP_047304071.1:p.Phe221Ser |
| lipoma-preferred partner isoform X6 | XP_047304061.1:p.Phe221= | XP_047304061.1:p.Phe221Ser |
| lipoma-preferred partner isoform X6 | XP_047304065.1:p.Phe221= | XP_047304065.1:p.Phe221Ser |
| lipoma-preferred partner isoform X6 | XP_047304058.1:p.Phe221= | XP_047304058.1:p.Phe221Ser |
| lipoma-preferred partner isoform X6 | XP_047304057.1:p.Phe221= | XP_047304057.1:p.Phe221Ser |
| lipoma-preferred partner isoform X6 | XP_047304060.1:p.Phe221= | XP_047304060.1:p.Phe221Ser |
| lipoma-preferred partner isoform X6 | XP_047304064.1:p.Phe221= | XP_047304064.1:p.Phe221Ser |
| lipoma-preferred partner isoform X6 | XP_047304062.1:p.Phe221= | XP_047304062.1:p.Phe221Ser |
| lipoma-preferred partner isoform X1 | XP_047304053.1:p.Phe285= | XP_047304053.1:p.Phe285Ser |
| lipoma-preferred partner isoform X6 | XP_047304070.1:p.Phe221= | XP_047304070.1:p.Phe221Ser |
| lipoma-preferred partner isoform X6 | XP_047304066.1:p.Phe221= | XP_047304066.1:p.Phe221Ser |
| lipoma-preferred partner isoform X6 | XP_047304069.1:p.Phe221= | XP_047304069.1:p.Phe221Ser |
| lipoma-preferred partner isoform X6 | XP_047304068.1:p.Phe221= | XP_047304068.1:p.Phe221Ser |
| lipoma-preferred partner isoform X6 | XP_047304067.1:p.Phe221= | XP_047304067.1:p.Phe221Ser |
| lipoma-preferred partner isoform X4 | XP_047304055.1:p.Phe244= | XP_047304055.1:p.Phe244Ser |
| lipoma-preferred partner isoform X6 | XP_047304063.1:p.Phe221= | XP_047304063.1:p.Phe221Ser |
| lipoma-preferred partner isoform X2 | XP_047304054.1:p.Phe266= | XP_047304054.1:p.Phe266Ser |
| lipoma-preferred partner isoform X7 | XP_047304072.1:p.Phe221= | XP_047304072.1:p.Phe221Ser |
| lipoma-preferred partner isoform X8 | XP_016861870.1:p.Phe221= | XP_016861870.1:p.Phe221Ser |
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 | ss2734268029 | Nov 08, 2017 (151) |
| 2 | gnomAD - Exomes | NC_000003.11 - 188327181 | 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).
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 rs1481164883
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
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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.
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.