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.
rs1488500922
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr1:150812104 (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
- G>A
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
G=0.5 (1/2, SGDP_PRJ)A=0.5 (1/2, SGDP_PRJ)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
- ARNT : Synonymous 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 |
|---|---|---|---|---|---|
| SGDP_PRJ | Global | Study-wide | 2 | G=0.5 | A=0.5 |
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 1 | NC_000001.11:g.150812104G>A |
| GRCh37.p13 chr 1 | NC_000001.10:g.150784580G>A |
| ARNT RefSeqGene | NG_028248.1:g.69665C>T |
| CTSK RefSeqGene | NG_011848.1:g.1233C>T |
Gene: ARNT, aryl hydrocarbon receptor nuclear translocator
(minus strand)
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| ARNT transcript variant 1 | NM_001668.4:c.2287C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform 1 | NP_001659.1:p.Leu763= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant 7 | NM_001350224.2:c.2260C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform 7 | NP_001337153.1:p.Leu754= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant 9 | NM_001350226.2:c.2281C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform 9 | NP_001337155.1:p.Leu761= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant 4 | NM_001197325.2:c.2239C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform 4 | NP_001184254.1:p.Leu747= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant 5 | NM_001286035.2:c.2245C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform 5 | NP_001272964.1:p.Leu749= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant 6 | NM_001286036.2:c.2281C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform 6 | NP_001272965.1:p.Leu761= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant 8 | NM_001350225.2:c.2284C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform 8 | NP_001337154.1:p.Leu762= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant 3 | NM_178427.3:c.2242C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform 3 | NP_848514.1:p.Leu748= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X1 | XM_017001288.3:c.2257C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X1 | XP_016856777.1:p.Leu753= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X2 | XM_017001289.2:c.2245C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X2 | XP_016856778.1:p.Leu749= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X3 | XM_047420692.1:c.2242C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X3 | XP_047276648.1:p.Leu748= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X4 | XM_017001290.3:c.2215C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X4 | XP_016856779.1:p.Leu739= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X5 | XM_017001291.2:c.2212C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X5 | XP_016856780.1:p.Leu738= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X6 | XM_047420694.1:c.2200C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X6 | XP_047276650.1:p.Leu734= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X7 | XM_047420697.1:c.2197C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X7 | XP_047276653.1:p.Leu733= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X8 | XM_017001292.2:c.2149C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X8 | XP_016856781.1:p.Leu717= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X9 | XM_047420700.1:c.2146C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X9 | XP_047276656.1:p.Leu716= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X10 | XM_047420701.1:c.2104C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X10 | XP_047276657.1:p.Leu702= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X11 | XM_017001293.2:c.2101C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X11 | XP_016856782.1:p.Leu701= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X12 | XM_005245151.3:c.2284C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X12 | XP_005245208.1:p.Leu762= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X13 | XM_011509543.4:c.2284C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X13 | XP_011507845.1:p.Leu762= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X14 | XM_047420709.1:c.2281C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X14 | XP_047276665.1:p.Leu761= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X15 | XM_005245153.2:c.2272C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X15 | XP_005245210.1:p.Leu758= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X16 | XM_047420711.1:c.2269C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X16 | XP_047276667.1:p.Leu757= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X17 | XM_047420712.1:c.2239C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X17 | XP_047276668.1:p.Leu747= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X18 | XM_047420713.1:c.2233C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X18 | XP_047276669.1:p.Leu745= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X19 | XM_047420715.1:c.2227C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X19 | XP_047276671.1:p.Leu743= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X20 | XM_047420716.1:c.2224C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X20 | XP_047276672.1:p.Leu742= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X21 | XM_011509546.3:c.2191C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X21 | XP_011507848.1:p.Leu731= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X22 | XM_005245157.2:c.2176C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X22 | XP_005245214.1:p.Leu726= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X23 | XM_017001294.2:c.2173C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X23 | XP_016856783.1:p.Leu725= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X24 | XM_017001295.2:c.2161C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X24 | XP_016856784.1:p.Leu721= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X25 | XM_047420719.1:c.2158C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X25 | XP_047276675.1:p.Leu720= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X26 | XM_017001296.2:c.2131C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X26 | XP_016856785.1:p.Leu711= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X27 | XM_047420727.1:c.2128C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X27 | XP_047276683.1:p.Leu710= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X28 | XM_047420734.1:c.2116C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X28 | XP_047276690.1:p.Leu706= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X29 | XM_047420740.1:c.2113C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X29 | XP_047276696.1:p.Leu705= | L (Leu) > L (Leu) | Synonymous Variant |
| ARNT transcript variant X30 | XM_047420743.1:c.2236C>T | L [CTG] > L [TTG] | Coding Sequence Variant |
| aryl hydrocarbon receptor nuclear translocator isoform X30 | XP_047276699.1:p.Leu746= | L (Leu) > L (Leu) | Synonymous 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 | G= | A |
|---|---|---|
| GRCh38.p14 chr 1 | NC_000001.11:g.150812104= | NC_000001.11:g.150812104G>A |
| GRCh37.p13 chr 1 | NC_000001.10:g.150784580= | NC_000001.10:g.150784580G>A |
| ARNT RefSeqGene | NG_028248.1:g.69665= | NG_028248.1:g.69665C>T |
| ARNT transcript variant 1 | NM_001668.4:c.2287= | NM_001668.4:c.2287C>T |
| ARNT transcript variant 1 | NM_001668.3:c.2287= | NM_001668.3:c.2287C>T |
| ARNT transcript variant 3 | NM_178427.3:c.2242= | NM_178427.3:c.2242C>T |
| ARNT transcript variant 3 | NM_178427.2:c.2242= | NM_178427.2:c.2242C>T |
| ARNT transcript variant 5 | NM_001286035.2:c.2245= | NM_001286035.2:c.2245C>T |
| ARNT transcript variant 5 | NM_001286035.1:c.2245= | NM_001286035.1:c.2245C>T |
| ARNT transcript variant 7 | NM_001350224.2:c.2260= | NM_001350224.2:c.2260C>T |
| ARNT transcript variant 7 | NM_001350224.1:c.2260= | NM_001350224.1:c.2260C>T |
| ARNT transcript variant 8 | NM_001350225.2:c.2284= | NM_001350225.2:c.2284C>T |
| ARNT transcript variant 8 | NM_001350225.1:c.2284= | NM_001350225.1:c.2284C>T |
| ARNT transcript variant 9 | NM_001350226.2:c.2281= | NM_001350226.2:c.2281C>T |
| ARNT transcript variant 9 | NM_001350226.1:c.2281= | NM_001350226.1:c.2281C>T |
| ARNT transcript variant 6 | NM_001286036.2:c.2281= | NM_001286036.2:c.2281C>T |
| ARNT transcript variant 6 | NM_001286036.1:c.2281= | NM_001286036.1:c.2281C>T |
| ARNT transcript variant 4 | NM_001197325.2:c.2239= | NM_001197325.2:c.2239C>T |
| ARNT transcript variant 4 | NM_001197325.1:c.2239= | NM_001197325.1:c.2239C>T |
| CTSK RefSeqGene | NG_011848.1:g.1233= | NG_011848.1:g.1233C>T |
| ARNT transcript variant X13 | XM_011509543.4:c.2284= | XM_011509543.4:c.2284C>T |
| ARNT transcript variant X8 | XM_011509543.3:c.2284= | XM_011509543.3:c.2284C>T |
| ARNT transcript variant X9 | XM_011509543.2:c.2284= | XM_011509543.2:c.2284C>T |
| ARNT transcript variant X3 | XM_011509543.1:c.2284= | XM_011509543.1:c.2284C>T |
| ARNT transcript variant X1 | XM_017001288.3:c.2257= | XM_017001288.3:c.2257C>T |
| ARNT transcript variant X1 | XM_017001288.2:c.2257= | XM_017001288.2:c.2257C>T |
| ARNT transcript variant X1 | XM_017001288.1:c.2257= | XM_017001288.1:c.2257C>T |
| ARNT transcript variant X12 | XM_005245151.3:c.2284= | XM_005245151.3:c.2284C>T |
| ARNT transcript variant X7 | XM_005245151.2:c.2284= | XM_005245151.2:c.2284C>T |
| ARNT transcript variant X8 | XM_005245151.1:c.2284= | XM_005245151.1:c.2284C>T |
| ARNT transcript variant X4 | XM_017001290.3:c.2215= | XM_017001290.3:c.2215C>T |
| ARNT transcript variant X3 | XM_017001290.2:c.2215= | XM_017001290.2:c.2215C>T |
| ARNT transcript variant X3 | XM_017001290.1:c.2215= | XM_017001290.1:c.2215C>T |
| ARNT transcript variant X21 | XM_011509546.3:c.2191= | XM_011509546.3:c.2191C>T |
| ARNT transcript variant X11 | XM_011509546.2:c.2191= | XM_011509546.2:c.2191C>T |
| ARNT transcript variant X14 | XM_011509546.1:c.2191= | XM_011509546.1:c.2191C>T |
| ARNT transcript variant X2 | XM_017001289.2:c.2245= | XM_017001289.2:c.2245C>T |
| ARNT transcript variant X2 | XM_017001289.1:c.2245= | XM_017001289.1:c.2245C>T |
| ARNT transcript variant X5 | XM_017001291.2:c.2212= | XM_017001291.2:c.2212C>T |
| ARNT transcript variant X4 | XM_017001291.1:c.2212= | XM_017001291.1:c.2212C>T |
| ARNT transcript variant X15 | XM_005245153.2:c.2272= | XM_005245153.2:c.2272C>T |
| ARNT transcript variant X9 | XM_005245153.1:c.2272= | XM_005245153.1:c.2272C>T |
| ARNT transcript variant X8 | XM_017001292.2:c.2149= | XM_017001292.2:c.2149C>T |
| ARNT transcript variant X5 | XM_017001292.1:c.2149= | XM_017001292.1:c.2149C>T |
| ARNT transcript variant X22 | XM_005245157.2:c.2176= | XM_005245157.2:c.2176C>T |
| ARNT transcript variant X12 | XM_005245157.1:c.2176= | XM_005245157.1:c.2176C>T |
| ARNT transcript variant X23 | XM_017001294.2:c.2173= | XM_017001294.2:c.2173C>T |
| ARNT transcript variant X13 | XM_017001294.1:c.2173= | XM_017001294.1:c.2173C>T |
| ARNT transcript variant X11 | XM_017001293.2:c.2101= | XM_017001293.2:c.2101C>T |
| ARNT transcript variant X6 | XM_017001293.1:c.2101= | XM_017001293.1:c.2101C>T |
| ARNT transcript variant X24 | XM_017001295.2:c.2161= | XM_017001295.2:c.2161C>T |
| ARNT transcript variant X14 | XM_017001295.1:c.2161= | XM_017001295.1:c.2161C>T |
| ARNT transcript variant X26 | XM_017001296.2:c.2131= | XM_017001296.2:c.2131C>T |
| ARNT transcript variant X15 | XM_017001296.1:c.2131= | XM_017001296.1:c.2131C>T |
| ARNT transcript variant X14 | XM_047420709.1:c.2281= | XM_047420709.1:c.2281C>T |
| ARNT transcript variant X17 | XM_047420712.1:c.2239= | XM_047420712.1:c.2239C>T |
| ARNT transcript variant X30 | XM_047420743.1:c.2236= | XM_047420743.1:c.2236C>T |
| ARNT transcript variant X18 | XM_047420713.1:c.2233= | XM_047420713.1:c.2233C>T |
| ARNT transcript variant X3 | XM_047420692.1:c.2242= | XM_047420692.1:c.2242C>T |
| ARNT transcript variant X16 | XM_047420711.1:c.2269= | XM_047420711.1:c.2269C>T |
| ARNT transcript variant X6 | XM_047420694.1:c.2200= | XM_047420694.1:c.2200C>T |
| ARNT transcript variant X7 | XM_047420697.1:c.2197= | XM_047420697.1:c.2197C>T |
| ARNT transcript variant X19 | XM_047420715.1:c.2227= | XM_047420715.1:c.2227C>T |
| ARNT transcript variant X20 | XM_047420716.1:c.2224= | XM_047420716.1:c.2224C>T |
| ARNT transcript variant X9 | XM_047420700.1:c.2146= | XM_047420700.1:c.2146C>T |
| ARNT transcript variant X10 | XM_047420701.1:c.2104= | XM_047420701.1:c.2104C>T |
| ARNT transcript variant X25 | XM_047420719.1:c.2158= | XM_047420719.1:c.2158C>T |
| ARNT transcript variant X27 | XM_047420727.1:c.2128= | XM_047420727.1:c.2128C>T |
| ARNT transcript variant X28 | XM_047420734.1:c.2116= | XM_047420734.1:c.2116C>T |
| ARNT transcript variant X29 | XM_047420740.1:c.2113= | XM_047420740.1:c.2113C>T |
| ARNT transcript variant 2 | NM_178426.1:c.*17= | NM_178426.1:c.*17C>T |
| aryl hydrocarbon receptor nuclear translocator isoform 1 | NP_001659.1:p.Leu763= | NP_001659.1:p.Leu763= |
| aryl hydrocarbon receptor nuclear translocator isoform 3 | NP_848514.1:p.Leu748= | NP_848514.1:p.Leu748= |
| aryl hydrocarbon receptor nuclear translocator isoform 5 | NP_001272964.1:p.Leu749= | NP_001272964.1:p.Leu749= |
| aryl hydrocarbon receptor nuclear translocator isoform 7 | NP_001337153.1:p.Leu754= | NP_001337153.1:p.Leu754= |
| aryl hydrocarbon receptor nuclear translocator isoform 8 | NP_001337154.1:p.Leu762= | NP_001337154.1:p.Leu762= |
| aryl hydrocarbon receptor nuclear translocator isoform 9 | NP_001337155.1:p.Leu761= | NP_001337155.1:p.Leu761= |
| aryl hydrocarbon receptor nuclear translocator isoform 6 | NP_001272965.1:p.Leu761= | NP_001272965.1:p.Leu761= |
| aryl hydrocarbon receptor nuclear translocator isoform 4 | NP_001184254.1:p.Leu747= | NP_001184254.1:p.Leu747= |
| aryl hydrocarbon receptor nuclear translocator isoform X13 | XP_011507845.1:p.Leu762= | XP_011507845.1:p.Leu762= |
| aryl hydrocarbon receptor nuclear translocator isoform X1 | XP_016856777.1:p.Leu753= | XP_016856777.1:p.Leu753= |
| aryl hydrocarbon receptor nuclear translocator isoform X12 | XP_005245208.1:p.Leu762= | XP_005245208.1:p.Leu762= |
| aryl hydrocarbon receptor nuclear translocator isoform X4 | XP_016856779.1:p.Leu739= | XP_016856779.1:p.Leu739= |
| aryl hydrocarbon receptor nuclear translocator isoform X21 | XP_011507848.1:p.Leu731= | XP_011507848.1:p.Leu731= |
| aryl hydrocarbon receptor nuclear translocator isoform X2 | XP_016856778.1:p.Leu749= | XP_016856778.1:p.Leu749= |
| aryl hydrocarbon receptor nuclear translocator isoform X5 | XP_016856780.1:p.Leu738= | XP_016856780.1:p.Leu738= |
| aryl hydrocarbon receptor nuclear translocator isoform X15 | XP_005245210.1:p.Leu758= | XP_005245210.1:p.Leu758= |
| aryl hydrocarbon receptor nuclear translocator isoform X8 | XP_016856781.1:p.Leu717= | XP_016856781.1:p.Leu717= |
| aryl hydrocarbon receptor nuclear translocator isoform X22 | XP_005245214.1:p.Leu726= | XP_005245214.1:p.Leu726= |
| aryl hydrocarbon receptor nuclear translocator isoform X23 | XP_016856783.1:p.Leu725= | XP_016856783.1:p.Leu725= |
| aryl hydrocarbon receptor nuclear translocator isoform X11 | XP_016856782.1:p.Leu701= | XP_016856782.1:p.Leu701= |
| aryl hydrocarbon receptor nuclear translocator isoform X24 | XP_016856784.1:p.Leu721= | XP_016856784.1:p.Leu721= |
| aryl hydrocarbon receptor nuclear translocator isoform X26 | XP_016856785.1:p.Leu711= | XP_016856785.1:p.Leu711= |
| aryl hydrocarbon receptor nuclear translocator isoform X14 | XP_047276665.1:p.Leu761= | XP_047276665.1:p.Leu761= |
| aryl hydrocarbon receptor nuclear translocator isoform X17 | XP_047276668.1:p.Leu747= | XP_047276668.1:p.Leu747= |
| aryl hydrocarbon receptor nuclear translocator isoform X30 | XP_047276699.1:p.Leu746= | XP_047276699.1:p.Leu746= |
| aryl hydrocarbon receptor nuclear translocator isoform X18 | XP_047276669.1:p.Leu745= | XP_047276669.1:p.Leu745= |
| aryl hydrocarbon receptor nuclear translocator isoform X3 | XP_047276648.1:p.Leu748= | XP_047276648.1:p.Leu748= |
| aryl hydrocarbon receptor nuclear translocator isoform X16 | XP_047276667.1:p.Leu757= | XP_047276667.1:p.Leu757= |
| aryl hydrocarbon receptor nuclear translocator isoform X6 | XP_047276650.1:p.Leu734= | XP_047276650.1:p.Leu734= |
| aryl hydrocarbon receptor nuclear translocator isoform X7 | XP_047276653.1:p.Leu733= | XP_047276653.1:p.Leu733= |
| aryl hydrocarbon receptor nuclear translocator isoform X19 | XP_047276671.1:p.Leu743= | XP_047276671.1:p.Leu743= |
| aryl hydrocarbon receptor nuclear translocator isoform X20 | XP_047276672.1:p.Leu742= | XP_047276672.1:p.Leu742= |
| aryl hydrocarbon receptor nuclear translocator isoform X9 | XP_047276656.1:p.Leu716= | XP_047276656.1:p.Leu716= |
| aryl hydrocarbon receptor nuclear translocator isoform X10 | XP_047276657.1:p.Leu702= | XP_047276657.1:p.Leu702= |
| aryl hydrocarbon receptor nuclear translocator isoform X25 | XP_047276675.1:p.Leu720= | XP_047276675.1:p.Leu720= |
| aryl hydrocarbon receptor nuclear translocator isoform X27 | XP_047276683.1:p.Leu710= | XP_047276683.1:p.Leu710= |
| aryl hydrocarbon receptor nuclear translocator isoform X28 | XP_047276690.1:p.Leu706= | XP_047276690.1:p.Leu706= |
| aryl hydrocarbon receptor nuclear translocator isoform X29 | XP_047276696.1:p.Leu705= | XP_047276696.1:p.Leu705= |
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#.
3 SubSNP,
1 Frequency
submissions
| No | Submitter | Submission ID | Date (Build) |
|---|---|---|---|
| 1 | GNOMAD | ss2731825567 | Nov 08, 2017 (151) |
| 2 | SGDP_PRJ | ss3849953679 | Apr 25, 2020 (154) |
| 3 | EVA | ss5321885019 | Oct 12, 2022 (156) |
| 4 | SGDP_PRJ | NC_000001.10 - 150784580 | Apr 25, 2020 (154) |
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).
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
No publications for rs1488500922
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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.