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.
rs1482376346
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr13:37021592 (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
- C>A
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
A=0.000011 (3/264690, TOPMED)A=0.00000 (0/10680, ALFA)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
- SUPT20H : Missense 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 | Alt HMOZ | HTRZ | HWEP |
|---|---|---|---|---|---|---|---|---|
| Total | Global | 10680 | C=1.00000 | A=0.00000 | 1.0 | 0.0 | 0.0 | N/A |
| European | Sub | 6962 | C=1.0000 | A=0.0000 | 1.0 | 0.0 | 0.0 | N/A |
| African | Sub | 2294 | C=1.0000 | A=0.0000 | 1.0 | 0.0 | 0.0 | N/A |
| African Others | Sub | 84 | C=1.00 | A=0.00 | 1.0 | 0.0 | 0.0 | N/A |
| African American | Sub | 2210 | C=1.0000 | A=0.0000 | 1.0 | 0.0 | 0.0 | N/A |
| Asian | Sub | 108 | C=1.000 | A=0.000 | 1.0 | 0.0 | 0.0 | N/A |
| East Asian | Sub | 84 | C=1.00 | A=0.00 | 1.0 | 0.0 | 0.0 | N/A |
| Other Asian | Sub | 24 | C=1.00 | A=0.00 | 1.0 | 0.0 | 0.0 | N/A |
| Latin American 1 | Sub | 146 | C=1.000 | A=0.000 | 1.0 | 0.0 | 0.0 | N/A |
| Latin American 2 | Sub | 610 | C=1.000 | A=0.000 | 1.0 | 0.0 | 0.0 | N/A |
| South Asian | Sub | 94 | C=1.00 | A=0.00 | 1.0 | 0.0 | 0.0 | N/A |
| Other | Sub | 466 | C=1.000 | A=0.000 | 1.0 | 0.0 | 0.0 | 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").
Download| Study | Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|---|
| TopMed | Global | Study-wide | 264690 | C=0.999989 | A=0.000011 |
| Allele Frequency Aggregator | Total | Global | 10680 | C=1.00000 | A=0.00000 |
| Allele Frequency Aggregator | European | Sub | 6962 | C=1.0000 | A=0.0000 |
| Allele Frequency Aggregator | African | Sub | 2294 | C=1.0000 | A=0.0000 |
| Allele Frequency Aggregator | Latin American 2 | Sub | 610 | C=1.000 | A=0.000 |
| Allele Frequency Aggregator | Other | Sub | 466 | C=1.000 | A=0.000 |
| Allele Frequency Aggregator | Latin American 1 | Sub | 146 | C=1.000 | A=0.000 |
| Allele Frequency Aggregator | Asian | Sub | 108 | C=1.000 | A=0.000 |
| Allele Frequency Aggregator | South Asian | Sub | 94 | C=1.00 | A=0.00 |
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 13 | NC_000013.11:g.37021592C>A |
| GRCh37.p13 chr 13 | NC_000013.10:g.37595729C>A |
Gene: SUPT20H, SPT20 homolog, SAGA complex component
(minus strand)
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| SUPT20H transcript variant 1 | NM_001014286.3:c.1672G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform a | NP_001014308.2:p.Ala558Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant 4 | NM_001278481.2:c.1675G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform b | NP_001265410.1:p.Ala559Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant 5 | NM_001278482.2:c.1675G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform b | NP_001265411.1:p.Ala559Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant 3 | NM_001278480.2:c.1909G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform c | NP_001265409.1:p.Ala637Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant 2 | NM_017569.4:c.1675G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform b | NP_060039.1:p.Ala559Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X42 | XM_047430465.1:c. | N/A | Genic Downstream Transcript Variant |
| SUPT20H transcript variant X43 | XM_047430466.1:c. | N/A | Genic Downstream Transcript Variant |
| SUPT20H transcript variant X44 | XM_047430467.1:c. | N/A | Genic Downstream Transcript Variant |
| SUPT20H transcript variant X45 | XM_047430468.1:c. | N/A | Genic Downstream Transcript Variant |
| SUPT20H transcript variant X46 | XM_047430469.1:c. | N/A | Genic Downstream Transcript Variant |
| SUPT20H transcript variant X47 | XM_047430470.1:c. | N/A | Genic Downstream Transcript Variant |
| SUPT20H transcript variant X1 | XM_005266447.3:c.1912G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X1 | XP_005266504.1:p.Ala638Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X2 | XM_005266449.5:c.1912G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X1 | XP_005266506.1:p.Ala638Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X3 | XM_005266451.5:c.1909G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X2 | XP_005266508.1:p.Ala637Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X4 | XM_047430444.1:c.1909G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X2 | XP_047286400.1:p.Ala637Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X5 | XM_005266454.5:c.1876G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X3 | XP_005266511.1:p.Ala626Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X6 | XM_005266456.5:c.1876G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X3 | XP_005266513.1:p.Ala626Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X7 | XM_005266455.3:c.1912G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X4 | XP_005266512.1:p.Ala638Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X8 | XM_005266457.5:c.1873G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X5 | XP_005266514.1:p.Ala625Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X9 | XM_017020653.3:c.1909G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X6 | XP_016876142.1:p.Ala637Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X10 | XM_005266458.5:c.1873G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X5 | XP_005266515.1:p.Ala625Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X11 | XM_047430445.1:c.1876G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X7 | XP_047286401.1:p.Ala626Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X12 | XM_047430447.1:c.1873G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X8 | XP_047286403.1:p.Ala625Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X13 | XM_047430448.1:c.1873G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X8 | XP_047286404.1:p.Ala625Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X14 | XM_005266460.3:c.1912G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X9 | XP_005266517.1:p.Ala638Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X15 | XM_047430449.1:c.1909G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X10 | XP_047286405.1:p.Ala637Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X16 | XM_047430450.1:c.1876G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X11 | XP_047286406.1:p.Ala626Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X17 | XM_005266461.4:c.1912G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X12 | XP_005266518.1:p.Ala638Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X18 | XM_047430451.1:c.1873G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X13 | XP_047286407.1:p.Ala625Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X19 | XM_047430452.1:c.1909G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X14 | XP_047286408.1:p.Ala637Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X20 | XM_047430453.1:c.1876G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X15 | XP_047286409.1:p.Ala626Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X21 | XM_047430454.1:c.1873G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X16 | XP_047286410.1:p.Ala625Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X22 | XM_005266462.5:c.1675G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X17 | XP_005266519.1:p.Ala559Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X23 | XM_047430456.1:c.1675G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X17 | XP_047286412.1:p.Ala559Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X24 | XM_047430457.1:c.1672G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X18 | XP_047286413.1:p.Ala558Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X25 | XM_017020654.2:c.1639G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X19 | XP_016876143.1:p.Ala547Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X26 | XM_047430458.1:c.1639G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X19 | XP_047286414.1:p.Ala547Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X27 | XM_005266464.4:c.1675G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X20 | XP_005266521.1:p.Ala559Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X28 | XM_017020655.2:c.1636G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X21 | XP_016876144.1:p.Ala546Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X29 | XM_017020657.3:c.1672G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X22 | XP_016876146.1:p.Ala558Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X30 | XM_047430459.1:c.1672G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X22 | XP_047286415.1:p.Ala558Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X31 | XM_047430460.1:c.1639G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X23 | XP_047286416.1:p.Ala547Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X32 | XM_024449379.2:c.1636G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X24 | XP_024305147.1:p.Ala546Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X33 | XM_005266465.4:c.1672G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X25 | XP_005266522.1:p.Ala558Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X34 | XM_047430462.1:c.1672G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X25 | XP_047286418.1:p.Ala558Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X35 | XM_017020658.2:c.1639G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X26 | XP_016876147.1:p.Ala547Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X36 | XM_005266467.4:c.1675G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X27 | XP_005266524.1:p.Ala559Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X37 | XM_017020659.2:c.1636G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X28 | XP_016876148.1:p.Ala546Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X38 | XM_017020660.3:c.1672G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X29 | XP_016876149.1:p.Ala558Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X39 | XM_047430463.1:c.1672G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X29 | XP_047286419.1:p.Ala558Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X40 | XM_047430464.1:c.1639G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X30 | XP_047286420.1:p.Ala547Ser | A (Ala) > S (Ser) | Missense Variant |
| SUPT20H transcript variant X41 | XM_017020661.2:c.1636G>T | A [GCT] > S [TCT] | Coding Sequence Variant |
| transcription factor SPT20 homolog isoform X31 | XP_016876150.1:p.Ala546Ser | A (Ala) > S (Ser) | Missense 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 | C= | A |
|---|---|---|
| GRCh38.p14 chr 13 | NC_000013.11:g.37021592= | NC_000013.11:g.37021592C>A |
| GRCh37.p13 chr 13 | NC_000013.10:g.37595729= | NC_000013.10:g.37595729C>A |
| SUPT20H transcript variant X2 | XM_005266449.5:c.1912= | XM_005266449.5:c.1912G>T |
| SUPT20H transcript variant X2 | XM_005266449.4:c.1912= | XM_005266449.4:c.1912G>T |
| SUPT20H transcript variant X2 | XM_005266449.3:c.1912= | XM_005266449.3:c.1912G>T |
| SUPT20H transcript variant X2 | XM_005266449.2:c.1912= | XM_005266449.2:c.1912G>T |
| SUPT20H transcript variant X3 | XM_005266449.1:c.1912= | XM_005266449.1:c.1912G>T |
| SUPT20H transcript variant X6 | XM_005266456.5:c.1876= | XM_005266456.5:c.1876G>T |
| SUPT20H transcript variant X8 | XM_005266456.4:c.1876= | XM_005266456.4:c.1876G>T |
| SUPT20H transcript variant X5 | XM_005266456.3:c.1876= | XM_005266456.3:c.1876G>T |
| SUPT20H transcript variant X9 | XM_005266456.2:c.1876= | XM_005266456.2:c.1876G>T |
| SUPT20H transcript variant X10 | XM_005266456.1:c.1876= | XM_005266456.1:c.1876G>T |
| SUPT20H transcript variant X10 | XM_005266458.5:c.1873= | XM_005266458.5:c.1873G>T |
| SUPT20H transcript variant X11 | XM_005266458.4:c.1873= | XM_005266458.4:c.1873G>T |
| SUPT20H transcript variant X8 | XM_005266458.3:c.1873= | XM_005266458.3:c.1873G>T |
| SUPT20H transcript variant X12 | XM_005266458.2:c.1873= | XM_005266458.2:c.1873G>T |
| SUPT20H transcript variant X12 | XM_005266458.1:c.1873= | XM_005266458.1:c.1873G>T |
| SUPT20H transcript variant X3 | XM_005266451.5:c.1909= | XM_005266451.5:c.1909G>T |
| SUPT20H transcript variant X5 | XM_005266451.4:c.1909= | XM_005266451.4:c.1909G>T |
| SUPT20H transcript variant X3 | XM_005266451.3:c.1909= | XM_005266451.3:c.1909G>T |
| SUPT20H transcript variant X5 | XM_005266451.2:c.1909= | XM_005266451.2:c.1909G>T |
| SUPT20H transcript variant X5 | XM_005266451.1:c.1909= | XM_005266451.1:c.1909G>T |
| SUPT20H transcript variant X5 | XM_005266454.5:c.1876= | XM_005266454.5:c.1876G>T |
| SUPT20H transcript variant X7 | XM_005266454.4:c.1876= | XM_005266454.4:c.1876G>T |
| SUPT20H transcript variant X4 | XM_005266454.3:c.1876= | XM_005266454.3:c.1876G>T |
| SUPT20H transcript variant X8 | XM_005266454.2:c.1876= | XM_005266454.2:c.1876G>T |
| SUPT20H transcript variant X8 | XM_005266454.1:c.1876= | XM_005266454.1:c.1876G>T |
| SUPT20H transcript variant X8 | XM_005266457.5:c.1873= | XM_005266457.5:c.1873G>T |
| SUPT20H transcript variant X10 | XM_005266457.4:c.1873= | XM_005266457.4:c.1873G>T |
| SUPT20H transcript variant X7 | XM_005266457.3:c.1873= | XM_005266457.3:c.1873G>T |
| SUPT20H transcript variant X11 | XM_005266457.2:c.1873= | XM_005266457.2:c.1873G>T |
| SUPT20H transcript variant X11 | XM_005266457.1:c.1873= | XM_005266457.1:c.1873G>T |
| SUPT20H transcript variant X22 | XM_005266462.5:c.1675= | XM_005266462.5:c.1675G>T |
| SUPT20H transcript variant X16 | XM_005266462.4:c.1675= | XM_005266462.4:c.1675G>T |
| SUPT20H transcript variant X16 | XM_005266462.3:c.1675= | XM_005266462.3:c.1675G>T |
| SUPT20H transcript variant X16 | XM_005266462.2:c.1675= | XM_005266462.2:c.1675G>T |
| SUPT20H transcript variant X16 | XM_005266462.1:c.1675= | XM_005266462.1:c.1675G>T |
| SUPT20H transcript variant X17 | XM_005266461.4:c.1912= | XM_005266461.4:c.1912G>T |
| SUPT20H transcript variant X15 | XM_005266461.3:c.1912= | XM_005266461.3:c.1912G>T |
| SUPT20H transcript variant X15 | XM_005266461.2:c.1912= | XM_005266461.2:c.1912G>T |
| SUPT20H transcript variant X15 | XM_005266461.1:c.1912= | XM_005266461.1:c.1912G>T |
| SUPT20H transcript variant 2 | NM_017569.4:c.1675= | NM_017569.4:c.1675G>T |
| SUPT20H transcript variant 2 | NM_017569.3:c.1675= | NM_017569.3:c.1675G>T |
| SUPT20H transcript variant X27 | XM_005266464.4:c.1675= | XM_005266464.4:c.1675G>T |
| SUPT20H transcript variant X18 | XM_005266464.3:c.1675= | XM_005266464.3:c.1675G>T |
| SUPT20H transcript variant X18 | XM_005266464.2:c.1675= | XM_005266464.2:c.1675G>T |
| SUPT20H transcript variant X18 | XM_005266464.1:c.1675= | XM_005266464.1:c.1675G>T |
| SUPT20H transcript variant X33 | XM_005266465.4:c.1672= | XM_005266465.4:c.1672G>T |
| SUPT20H transcript variant X23 | XM_005266465.3:c.1672= | XM_005266465.3:c.1672G>T |
| SUPT20H transcript variant X18 | XM_005266465.2:c.1672= | XM_005266465.2:c.1672G>T |
| SUPT20H transcript variant X19 | XM_005266465.1:c.1672= | XM_005266465.1:c.1672G>T |
| SUPT20H transcript variant X36 | XM_005266467.4:c.1675= | XM_005266467.4:c.1675G>T |
| SUPT20H transcript variant X25 | XM_005266467.3:c.1675= | XM_005266467.3:c.1675G>T |
| SUPT20H transcript variant X21 | XM_005266467.2:c.1675= | XM_005266467.2:c.1675G>T |
| SUPT20H transcript variant X21 | XM_005266467.1:c.1675= | XM_005266467.1:c.1675G>T |
| SUPT20H transcript variant X1 | XM_005266447.3:c.1912= | XM_005266447.3:c.1912G>T |
| SUPT20H transcript variant X1 | XM_005266447.2:c.1912= | XM_005266447.2:c.1912G>T |
| SUPT20H transcript variant X1 | XM_005266447.1:c.1912= | XM_005266447.1:c.1912G>T |
| SUPT20H transcript variant X7 | XM_005266455.3:c.1912= | XM_005266455.3:c.1912G>T |
| SUPT20H transcript variant X9 | XM_005266455.2:c.1912= | XM_005266455.2:c.1912G>T |
| SUPT20H transcript variant X9 | XM_005266455.1:c.1912= | XM_005266455.1:c.1912G>T |
| SUPT20H transcript variant X9 | XM_017020653.3:c.1909= | XM_017020653.3:c.1909G>T |
| SUPT20H transcript variant X12 | XM_017020653.2:c.1909= | XM_017020653.2:c.1909G>T |
| SUPT20H transcript variant X9 | XM_017020653.1:c.1909= | XM_017020653.1:c.1909G>T |
| SUPT20H transcript variant X14 | XM_005266460.3:c.1912= | XM_005266460.3:c.1912G>T |
| SUPT20H transcript variant X13 | XM_005266460.2:c.1912= | XM_005266460.2:c.1912G>T |
| SUPT20H transcript variant X14 | XM_005266460.1:c.1912= | XM_005266460.1:c.1912G>T |
| SUPT20H transcript variant 1 | NM_001014286.3:c.1672= | NM_001014286.3:c.1672G>T |
| SUPT20H transcript variant 1 | NM_001014286.2:c.1672= | NM_001014286.2:c.1672G>T |
| SUPT20H transcript variant X29 | XM_017020657.3:c.1672= | XM_017020657.3:c.1672G>T |
| SUPT20H transcript variant X21 | XM_017020657.2:c.1672= | XM_017020657.2:c.1672G>T |
| SUPT20H transcript variant X17 | XM_017020657.1:c.1672= | XM_017020657.1:c.1672G>T |
| SUPT20H transcript variant X38 | XM_017020660.3:c.1672= | XM_017020660.3:c.1672G>T |
| SUPT20H transcript variant X27 | XM_017020660.2:c.1672= | XM_017020660.2:c.1672G>T |
| SUPT20H transcript variant X22 | XM_017020660.1:c.1672= | XM_017020660.1:c.1672G>T |
| SUPT20H transcript variant 5 | NM_001278482.2:c.1675= | NM_001278482.2:c.1675G>T |
| SUPT20H transcript variant 5 | NM_001278482.1:c.1675= | NM_001278482.1:c.1675G>T |
| SUPT20H transcript variant 3 | NM_001278480.2:c.1909= | NM_001278480.2:c.1909G>T |
| SUPT20H transcript variant 3 | NM_001278480.1:c.1909= | NM_001278480.1:c.1909G>T |
| SUPT20H transcript variant X25 | XM_017020654.2:c.1639= | XM_017020654.2:c.1639G>T |
| SUPT20H transcript variant X17 | XM_017020654.1:c.1639= | XM_017020654.1:c.1639G>T |
| SUPT20H transcript variant X28 | XM_017020655.2:c.1636= | XM_017020655.2:c.1636G>T |
| SUPT20H transcript variant X19 | XM_017020655.1:c.1636= | XM_017020655.1:c.1636G>T |
| SUPT20H transcript variant X32 | XM_024449379.2:c.1636= | XM_024449379.2:c.1636G>T |
| SUPT20H transcript variant X22 | XM_024449379.1:c.1636= | XM_024449379.1:c.1636G>T |
| SUPT20H transcript variant 4 | NM_001278481.2:c.1675= | NM_001278481.2:c.1675G>T |
| SUPT20H transcript variant 4 | NM_001278481.1:c.1675= | NM_001278481.1:c.1675G>T |
| SUPT20H transcript variant X35 | XM_017020658.2:c.1639= | XM_017020658.2:c.1639G>T |
| SUPT20H transcript variant X24 | XM_017020658.1:c.1639= | XM_017020658.1:c.1639G>T |
| SUPT20H transcript variant X37 | XM_017020659.2:c.1636= | XM_017020659.2:c.1636G>T |
| SUPT20H transcript variant X26 | XM_017020659.1:c.1636= | XM_017020659.1:c.1636G>T |
| SUPT20H transcript variant X41 | XM_017020661.2:c.1636= | XM_017020661.2:c.1636G>T |
| SUPT20H transcript variant X28 | XM_017020661.1:c.1636= | XM_017020661.1:c.1636G>T |
| SUPT20H transcript variant X4 | XM_047430444.1:c.1909= | XM_047430444.1:c.1909G>T |
| SUPT20H transcript variant X13 | XM_047430448.1:c.1873= | XM_047430448.1:c.1873G>T |
| SUPT20H transcript variant X15 | XM_047430449.1:c.1909= | XM_047430449.1:c.1909G>T |
| SUPT20H transcript variant X11 | XM_047430445.1:c.1876= | XM_047430445.1:c.1876G>T |
| SUPT20H transcript variant X12 | XM_047430447.1:c.1873= | XM_047430447.1:c.1873G>T |
| SUPT20H transcript variant X16 | XM_047430450.1:c.1876= | XM_047430450.1:c.1876G>T |
| SUPT20H transcript variant X19 | XM_047430452.1:c.1909= | XM_047430452.1:c.1909G>T |
| SUPT20H transcript variant X18 | XM_047430451.1:c.1873= | XM_047430451.1:c.1873G>T |
| SUPT20H transcript variant X23 | XM_047430456.1:c.1675= | XM_047430456.1:c.1675G>T |
| SUPT20H transcript variant X24 | XM_047430457.1:c.1672= | XM_047430457.1:c.1672G>T |
| SUPT20H transcript variant X20 | XM_047430453.1:c.1876= | XM_047430453.1:c.1876G>T |
| SUPT20H transcript variant X21 | XM_047430454.1:c.1873= | XM_047430454.1:c.1873G>T |
| SUPT20H transcript variant X26 | XM_047430458.1:c.1639= | XM_047430458.1:c.1639G>T |
| SUPT20H transcript variant X30 | XM_047430459.1:c.1672= | XM_047430459.1:c.1672G>T |
| SUPT20H transcript variant X34 | XM_047430462.1:c.1672= | XM_047430462.1:c.1672G>T |
| SUPT20H transcript variant X39 | XM_047430463.1:c.1672= | XM_047430463.1:c.1672G>T |
| SUPT20H transcript variant X31 | XM_047430460.1:c.1639= | XM_047430460.1:c.1639G>T |
| SUPT20H transcript variant X40 | XM_047430464.1:c.1639= | XM_047430464.1:c.1639G>T |
| transcription factor SPT20 homolog isoform X1 | XP_005266506.1:p.Ala638= | XP_005266506.1:p.Ala638Ser |
| transcription factor SPT20 homolog isoform X3 | XP_005266513.1:p.Ala626= | XP_005266513.1:p.Ala626Ser |
| transcription factor SPT20 homolog isoform X5 | XP_005266515.1:p.Ala625= | XP_005266515.1:p.Ala625Ser |
| transcription factor SPT20 homolog isoform X2 | XP_005266508.1:p.Ala637= | XP_005266508.1:p.Ala637Ser |
| transcription factor SPT20 homolog isoform X3 | XP_005266511.1:p.Ala626= | XP_005266511.1:p.Ala626Ser |
| transcription factor SPT20 homolog isoform X5 | XP_005266514.1:p.Ala625= | XP_005266514.1:p.Ala625Ser |
| transcription factor SPT20 homolog isoform X17 | XP_005266519.1:p.Ala559= | XP_005266519.1:p.Ala559Ser |
| transcription factor SPT20 homolog isoform X12 | XP_005266518.1:p.Ala638= | XP_005266518.1:p.Ala638Ser |
| transcription factor SPT20 homolog isoform b | NP_060039.1:p.Ala559= | NP_060039.1:p.Ala559Ser |
| transcription factor SPT20 homolog isoform X20 | XP_005266521.1:p.Ala559= | XP_005266521.1:p.Ala559Ser |
| transcription factor SPT20 homolog isoform X25 | XP_005266522.1:p.Ala558= | XP_005266522.1:p.Ala558Ser |
| transcription factor SPT20 homolog isoform X27 | XP_005266524.1:p.Ala559= | XP_005266524.1:p.Ala559Ser |
| transcription factor SPT20 homolog isoform X1 | XP_005266504.1:p.Ala638= | XP_005266504.1:p.Ala638Ser |
| transcription factor SPT20 homolog isoform X4 | XP_005266512.1:p.Ala638= | XP_005266512.1:p.Ala638Ser |
| transcription factor SPT20 homolog isoform X6 | XP_016876142.1:p.Ala637= | XP_016876142.1:p.Ala637Ser |
| transcription factor SPT20 homolog isoform X9 | XP_005266517.1:p.Ala638= | XP_005266517.1:p.Ala638Ser |
| transcription factor SPT20 homolog isoform a | NP_001014308.2:p.Ala558= | NP_001014308.2:p.Ala558Ser |
| transcription factor SPT20 homolog isoform X22 | XP_016876146.1:p.Ala558= | XP_016876146.1:p.Ala558Ser |
| transcription factor SPT20 homolog isoform X29 | XP_016876149.1:p.Ala558= | XP_016876149.1:p.Ala558Ser |
| transcription factor SPT20 homolog isoform b | NP_001265411.1:p.Ala559= | NP_001265411.1:p.Ala559Ser |
| transcription factor SPT20 homolog isoform c | NP_001265409.1:p.Ala637= | NP_001265409.1:p.Ala637Ser |
| transcription factor SPT20 homolog isoform X19 | XP_016876143.1:p.Ala547= | XP_016876143.1:p.Ala547Ser |
| transcription factor SPT20 homolog isoform X21 | XP_016876144.1:p.Ala546= | XP_016876144.1:p.Ala546Ser |
| transcription factor SPT20 homolog isoform X24 | XP_024305147.1:p.Ala546= | XP_024305147.1:p.Ala546Ser |
| transcription factor SPT20 homolog isoform b | NP_001265410.1:p.Ala559= | NP_001265410.1:p.Ala559Ser |
| transcription factor SPT20 homolog isoform X26 | XP_016876147.1:p.Ala547= | XP_016876147.1:p.Ala547Ser |
| transcription factor SPT20 homolog isoform X28 | XP_016876148.1:p.Ala546= | XP_016876148.1:p.Ala546Ser |
| transcription factor SPT20 homolog isoform X31 | XP_016876150.1:p.Ala546= | XP_016876150.1:p.Ala546Ser |
| transcription factor SPT20 homolog isoform X2 | XP_047286400.1:p.Ala637= | XP_047286400.1:p.Ala637Ser |
| transcription factor SPT20 homolog isoform X8 | XP_047286404.1:p.Ala625= | XP_047286404.1:p.Ala625Ser |
| transcription factor SPT20 homolog isoform X10 | XP_047286405.1:p.Ala637= | XP_047286405.1:p.Ala637Ser |
| transcription factor SPT20 homolog isoform X7 | XP_047286401.1:p.Ala626= | XP_047286401.1:p.Ala626Ser |
| transcription factor SPT20 homolog isoform X8 | XP_047286403.1:p.Ala625= | XP_047286403.1:p.Ala625Ser |
| transcription factor SPT20 homolog isoform X11 | XP_047286406.1:p.Ala626= | XP_047286406.1:p.Ala626Ser |
| transcription factor SPT20 homolog isoform X14 | XP_047286408.1:p.Ala637= | XP_047286408.1:p.Ala637Ser |
| transcription factor SPT20 homolog isoform X13 | XP_047286407.1:p.Ala625= | XP_047286407.1:p.Ala625Ser |
| transcription factor SPT20 homolog isoform X17 | XP_047286412.1:p.Ala559= | XP_047286412.1:p.Ala559Ser |
| transcription factor SPT20 homolog isoform X18 | XP_047286413.1:p.Ala558= | XP_047286413.1:p.Ala558Ser |
| transcription factor SPT20 homolog isoform X15 | XP_047286409.1:p.Ala626= | XP_047286409.1:p.Ala626Ser |
| transcription factor SPT20 homolog isoform X16 | XP_047286410.1:p.Ala625= | XP_047286410.1:p.Ala625Ser |
| transcription factor SPT20 homolog isoform X19 | XP_047286414.1:p.Ala547= | XP_047286414.1:p.Ala547Ser |
| transcription factor SPT20 homolog isoform X22 | XP_047286415.1:p.Ala558= | XP_047286415.1:p.Ala558Ser |
| transcription factor SPT20 homolog isoform X25 | XP_047286418.1:p.Ala558= | XP_047286418.1:p.Ala558Ser |
| transcription factor SPT20 homolog isoform X29 | XP_047286419.1:p.Ala558= | XP_047286419.1:p.Ala558Ser |
| transcription factor SPT20 homolog isoform X23 | XP_047286416.1:p.Ala547= | XP_047286416.1:p.Ala547Ser |
| transcription factor SPT20 homolog isoform X30 | XP_047286420.1:p.Ala547= | XP_047286420.1:p.Ala547Ser |
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#.
2 SubSNP,
2 Frequency
submissions
| No | Submitter | Submission ID | Date (Build) |
|---|---|---|---|
| 1 | GNOMAD | ss2740370116 | Nov 08, 2017 (151) |
| 2 | TOPMED | ss4943090784 | Apr 27, 2021 (155) |
| 3 | TopMed | NC_000013.11 - 37021592 | Apr 27, 2021 (155) |
| 4 | ALFA | NC_000013.11 - 37021592 | Apr 27, 2021 (155) |
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 rs1482376346
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.