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.
rs1481119446
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr7:108182794 (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>G
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
- G=0.000004 (1/251472, GnomAD_exome)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
- NRCAM : Missense Variant
- Publications
- 0 citations
- Genomic View
- See rs on genome
Help
Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").
Download| Study | Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|---|
| gnomAD - Exomes | Global | Study-wide | 251472 | T=0.999996 | G=0.000004 |
| gnomAD - Exomes | European | Sub | 135404 | T=1.000000 | G=0.000000 |
| gnomAD - Exomes | Asian | Sub | 49006 | T=1.00000 | G=0.00000 |
| gnomAD - Exomes | American | Sub | 34588 | T=0.99997 | G=0.00003 |
| gnomAD - Exomes | African | Sub | 16256 | T=1.00000 | G=0.00000 |
| gnomAD - Exomes | Ashkenazi Jewish | Sub | 10080 | T=1.00000 | G=0.00000 |
| gnomAD - Exomes | Other | Sub | 6138 | T=1.0000 | G=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 7 | NC_000007.14:g.108182794T>G |
| GRCh37.p13 chr 7 | NC_000007.13:g.107823238T>G |
| NRCAM RefSeqGene | NG_029898.2:g.278924A>C |
Gene: NRCAM, neuronal cell adhesion molecule
(minus strand)
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| NRCAM transcript variant 54 | NM_001371142.1:c.2086A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform Y | NP_001358071.1:p.Thr696Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 68 | NM_001371159.1:c.2401A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform ll precursor | NP_001358088.1:p.Thr801Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 43 | NM_001371154.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform O precursor | NP_001358083.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 61 | NM_001371160.1:c.2413A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform ff precursor | NP_001358089.1:p.Thr805Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 32 | NM_001371132.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform J precursor | NP_001358061.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 7 | NM_001371131.1:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform A precursor | NP_001358060.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 41 | NM_001371153.1:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform N precursor | NP_001358082.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 27 | NM_001371126.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform H precursor | NP_001358055.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 22 | NM_001371181.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform E precursor | NP_001358110.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 44 | NM_001371166.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform O precursor | NP_001358095.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 25 | NM_001371149.1:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform G precursor | NP_001358078.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 37 | NM_001371164.1:c.2086A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform L | NP_001358093.1:p.Thr696Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 60 | NM_001371158.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform ee precursor | NP_001358087.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 66 | NM_001371175.1:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform kk precursor | NP_001358104.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 31 | NM_001371129.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform J precursor | NP_001358058.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 56 | NM_001371146.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform aa precursor | NP_001358075.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 30 | NM_001371147.1:c.2086A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform I | NP_001358076.1:p.Thr696Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 35 | NM_001371176.1:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform K precursor | NP_001358105.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 23 | NM_001371162.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform F precursor | NP_001358091.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 46 | NM_001371127.1:c.2428A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform Q precursor | NP_001358056.1:p.Thr810Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 38 | NM_001371148.1:c.2113A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform M | NP_001358077.1:p.Thr705Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 13 | NM_001371144.1:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform D precursor | NP_001358073.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 9 | NM_001371151.1:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform B precursor | NP_001358080.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 24 | NM_001371123.1:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform G precursor | NP_001358052.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 33 | NM_001371130.1:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform K precursor | NP_001358059.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 62 | NM_001371169.1:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform gg precursor | NP_001358098.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 21 | NM_001371177.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform E precursor | NP_001358106.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 64 | NM_001371173.1:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform ii precursor | NP_001358102.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 28 | NM_001371172.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform H precursor | NP_001358101.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 11 | NM_001371178.1:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform B precursor | NP_001358107.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 52 | NM_001371140.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform W precursor | NP_001358069.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 45 | NM_001371119.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform P precursor | NP_001358048.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 39 | NM_001371179.1:c.2113A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform M | NP_001358108.1:p.Thr705Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 12 | NM_001371128.1:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform D precursor | NP_001358057.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 26 | NM_001371124.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform H precursor | NP_001358053.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 49 | NM_001371136.1:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform T precursor | NP_001358065.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 14 | NM_001371168.1:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform D precursor | NP_001358097.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 15 | NM_001371122.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform E precursor | NP_001358051.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 55 | NM_001371145.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform Z precursor | NP_001358074.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 48 | NM_001371135.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform S precursor | NP_001358064.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 65 | NM_001371174.1:c.2401A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform jj precursor | NP_001358103.1:p.Thr801Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 36 | NM_001371143.1:c.2086A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform L | NP_001358072.1:p.Thr696Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 58 | NM_001371156.1:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform cc precursor | NP_001358085.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 47 | NM_001371134.1:c.2380A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform R precursor | NP_001358063.1:p.Thr794Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 20 | NM_001371167.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform E precursor | NP_001358096.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 10 | NM_001371171.1:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform B precursor | NP_001358100.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 40 | NM_001371180.1:c.2113A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform M | NP_001358109.1:p.Thr705Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 17 | NM_001371155.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform E precursor | NP_001358084.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 67 | NM_001371182.1:c.2326A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform mm precursor | NP_001358111.1:p.Thr776Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 29 | NM_001371125.1:c.2086A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform I | NP_001358054.1:p.Thr696Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 34 | NM_001371152.1:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform K precursor | NP_001358081.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 63 | NM_001371170.1:c.2113A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform hh | NP_001358099.1:p.Thr705Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 50 | NM_001371137.1:c.1474A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform U | NP_001358066.1:p.Thr492Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 16 | NM_001371139.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform E precursor | NP_001358068.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 57 | NM_001371150.1:c.2401A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform bb precursor | NP_001358079.1:p.Thr801Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 8 | NM_001371133.1:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform B precursor | NP_001358062.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 18 | NM_001371163.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform E precursor | NP_001358092.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 59 | NM_001371157.1:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform dd precursor | NP_001358086.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 42 | NM_001371161.1:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform N precursor | NP_001358090.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 19 | NM_001371165.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform E precursor | NP_001358094.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 53 | NM_001371141.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X precursor | NP_001358070.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 51 | NM_001371138.1:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform V precursor | NP_001358067.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 1 | NM_001037132.4:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform A precursor | NP_001032209.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 2 | NM_005010.5:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform B precursor | NP_005001.3:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 4 | NM_001193582.2:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform D precursor | NP_001180511.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 6 | NM_001193584.2:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform F precursor | NP_001180513.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 5 | NM_001193583.2:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform E precursor | NP_001180512.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant 69 | NR_163867.1:n.2899A>C | N/A | Non Coding Transcript Variant |
| NRCAM transcript variant 73 | NR_163871.1:n.2978A>C | N/A | Non Coding Transcript Variant |
| NRCAM transcript variant 71 | NR_163869.1:n.2899A>C | N/A | Non Coding Transcript Variant |
| NRCAM transcript variant 70 | NR_163868.1:n.2899A>C | N/A | Non Coding Transcript Variant |
| NRCAM transcript variant 72 | NR_163870.1:n.2980A>C | N/A | Non Coding Transcript Variant |
| NRCAM transcript variant X1 | XM_011516253.3:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X1 | XP_011514555.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X2 | XM_011516255.2:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X1 | XP_011514557.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X3 | XM_006716003.3:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X2 | XP_006716066.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X4 | XM_011516257.3:c.2413A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X3 | XP_011514559.1:p.Thr805Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X5 | XM_011516258.2:c.2413A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X3 | XP_011514560.1:p.Thr805Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X6 | XM_011516259.3:c.2401A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X4 | XP_011514561.1:p.Thr801Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X7 | XM_017012236.3:c.2401A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X5 | XP_016867725.1:p.Thr801Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X8 | XM_011516261.3:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X6 | XP_011514563.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X9 | XM_011516262.3:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X7 | XP_011514564.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X10 | XM_017012238.3:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X8 | XP_016867727.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X11 | XM_047420417.1:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X9 | XP_047276373.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X12 | XM_017012239.3:c.2356A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X10 | XP_016867728.1:p.Thr786Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X13 | XM_047420418.1:c.2344A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X11 | XP_047276374.1:p.Thr782Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X14 | XM_011516265.4:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X12 | XP_011514567.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X15 | XM_011516267.3:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X13 | XP_011514569.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X16 | XM_006716012.3:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X14 | XP_006716075.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X17 | XM_011516268.3:c.2143A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X15 | XP_011514570.1:p.Thr715Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X18 | XM_011516269.3:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X16 | XP_011514571.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X19 | XM_017012246.3:c.2401A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X17 | XP_016867735.1:p.Thr801Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X20 | XM_006716014.3:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X18 | XP_006716077.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X21 | XM_011516270.3:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X19 | XP_011514572.1:p.Thr811Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X22 | XM_047420419.1:c.2401A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X20 | XP_047276375.1:p.Thr801Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X23 | XM_017012247.3:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X21 | XP_016867736.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X24 | XM_017012248.3:c.2401A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X22 | XP_016867737.1:p.Thr801Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X25 | XM_017012251.3:c.2401A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X23 | XP_016867740.1:p.Thr801Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X26 | XM_024446777.2:c.2413A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X24 | XP_024302545.1:p.Thr805Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X27 | XM_047420420.1:c.2374A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X25 | XP_047276376.1:p.Thr792Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X28 | XM_024446778.2:c.2383A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X26 | XP_024302546.1:p.Thr795Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X29 | XM_047420421.1:c.2344A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X27 | XP_047276377.1:p.Thr782Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X30 | XM_047420422.1:c.2326A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X28 | XP_047276378.1:p.Thr776Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X31 | XM_047420423.1:c.2344A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X29 | XP_047276379.1:p.Thr782Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X32 | XM_047420424.1:c.2356A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X30 | XP_047276380.1:p.Thr786Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X33 | XM_024446779.2:c.2326A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X31 | XP_024302547.1:p.Thr776Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X34 | XM_047420425.1:c.2326A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X32 | XP_047276381.1:p.Thr776Pro | T (Thr) > P (Pro) | Missense Variant |
| NRCAM transcript variant X35 | XM_024446780.2:c.2431A>C | T [ACG] > P [CCG] | Coding Sequence Variant |
| neuronal cell adhesion molecule isoform X33 | XP_024302548.1:p.Thr811Pro | T (Thr) > P (Pro) | 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 | T= | G |
|---|---|---|
| GRCh38.p14 chr 7 | NC_000007.14:g.108182794= | NC_000007.14:g.108182794T>G |
| GRCh37.p13 chr 7 | NC_000007.13:g.107823238= | NC_000007.13:g.107823238T>G |
| NRCAM RefSeqGene | NG_029898.2:g.278924= | NG_029898.2:g.278924A>C |
| NRCAM transcript variant 2 | NM_005010.5:c.2383= | NM_005010.5:c.2383A>C |
| NRCAM transcript variant 2 | NM_005010.4:c.2383= | NM_005010.4:c.2383A>C |
| NRCAM transcript variant 1 | NM_001037132.4:c.2431= | NM_001037132.4:c.2431A>C |
| NRCAM transcript variant 1 | NM_001037132.3:c.2431= | NM_001037132.3:c.2431A>C |
| NRCAM transcript variant 1 | NM_001037132.2:c.2431= | NM_001037132.2:c.2431A>C |
| NRCAM transcript variant 4 | NM_001193582.2:c.2431= | NM_001193582.2:c.2431A>C |
| NRCAM transcript variant 4 | NM_001193582.1:c.2431= | NM_001193582.1:c.2431A>C |
| NRCAM transcript variant 5 | NM_001193583.2:c.2374= | NM_001193583.2:c.2374A>C |
| NRCAM transcript variant 5 | NM_001193583.1:c.2374= | NM_001193583.1:c.2374A>C |
| NRCAM transcript variant 6 | NM_001193584.2:c.2374= | NM_001193584.2:c.2374A>C |
| NRCAM transcript variant 6 | NM_001193584.1:c.2374= | NM_001193584.1:c.2374A>C |
| NRCAM transcript variant 27 | NM_001371126.1:c.2374= | NM_001371126.1:c.2374A>C |
| NRCAM transcript variant 18 | NM_001371163.1:c.2374= | NM_001371163.1:c.2374A>C |
| NRCAM transcript variant 7 | NM_001371131.1:c.2431= | NM_001371131.1:c.2431A>C |
| NRCAM transcript variant 70 | NR_163868.1:n.2899= | NR_163868.1:n.2899A>C |
| NRCAM transcript variant 58 | NM_001371156.1:c.2431= | NM_001371156.1:c.2431A>C |
| NRCAM transcript variant 13 | NM_001371144.1:c.2431= | NM_001371144.1:c.2431A>C |
| NRCAM transcript variant 62 | NM_001371169.1:c.2431= | NM_001371169.1:c.2431A>C |
| NRCAM transcript variant 28 | NM_001371172.1:c.2374= | NM_001371172.1:c.2374A>C |
| NRCAM transcript variant 56 | NM_001371146.1:c.2374= | NM_001371146.1:c.2374A>C |
| NRCAM transcript variant 8 | NM_001371133.1:c.2383= | NM_001371133.1:c.2383A>C |
| NRCAM transcript variant 71 | NR_163869.1:n.2899= | NR_163869.1:n.2899A>C |
| NRCAM transcript variant 14 | NM_001371168.1:c.2431= | NM_001371168.1:c.2431A>C |
| NRCAM transcript variant 41 | NM_001371153.1:c.2431= | NM_001371153.1:c.2431A>C |
| NRCAM transcript variant 12 | NM_001371128.1:c.2431= | NM_001371128.1:c.2431A>C |
| NRCAM transcript variant 51 | NM_001371138.1:c.2431= | NM_001371138.1:c.2431A>C |
| NRCAM transcript variant 19 | NM_001371165.1:c.2374= | NM_001371165.1:c.2374A>C |
| NRCAM transcript variant 16 | NM_001371139.1:c.2374= | NM_001371139.1:c.2374A>C |
| NRCAM transcript variant 60 | NM_001371158.1:c.2374= | NM_001371158.1:c.2374A>C |
| NRCAM transcript variant 17 | NM_001371155.1:c.2374= | NM_001371155.1:c.2374A>C |
| NRCAM transcript variant 45 | NM_001371119.1:c.2374= | NM_001371119.1:c.2374A>C |
| NRCAM transcript variant 26 | NM_001371124.1:c.2374= | NM_001371124.1:c.2374A>C |
| NRCAM transcript variant 55 | NM_001371145.1:c.2374= | NM_001371145.1:c.2374A>C |
| NRCAM transcript variant 20 | NM_001371167.1:c.2374= | NM_001371167.1:c.2374A>C |
| NRCAM transcript variant 23 | NM_001371162.1:c.2374= | NM_001371162.1:c.2374A>C |
| NRCAM transcript variant 73 | NR_163871.1:n.2978= | NR_163871.1:n.2978A>C |
| NRCAM transcript variant 49 | NM_001371136.1:c.2383= | NM_001371136.1:c.2383A>C |
| NRCAM transcript variant 32 | NM_001371132.1:c.2374= | NM_001371132.1:c.2374A>C |
| NRCAM transcript variant 52 | NM_001371140.1:c.2374= | NM_001371140.1:c.2374A>C |
| NRCAM transcript variant 10 | NM_001371171.1:c.2383= | NM_001371171.1:c.2383A>C |
| NRCAM transcript variant 36 | NM_001371143.1:c.2086= | NM_001371143.1:c.2086A>C |
| NRCAM transcript variant 25 | NM_001371149.1:c.2431= | NM_001371149.1:c.2431A>C |
| NRCAM transcript variant 69 | NR_163867.1:n.2899= | NR_163867.1:n.2899A>C |
| NRCAM transcript variant 72 | NR_163870.1:n.2980= | NR_163870.1:n.2980A>C |
| NRCAM transcript variant 46 | NM_001371127.1:c.2428= | NM_001371127.1:c.2428A>C |
| NRCAM transcript variant 33 | NM_001371130.1:c.2383= | NM_001371130.1:c.2383A>C |
| NRCAM transcript variant 57 | NM_001371150.1:c.2401= | NM_001371150.1:c.2401A>C |
| NRCAM transcript variant 37 | NM_001371164.1:c.2086= | NM_001371164.1:c.2086A>C |
| NRCAM transcript variant 64 | NM_001371173.1:c.2431= | NM_001371173.1:c.2431A>C |
| NRCAM transcript variant 59 | NM_001371157.1:c.2383= | NM_001371157.1:c.2383A>C |
| NRCAM transcript variant 53 | NM_001371141.1:c.2374= | NM_001371141.1:c.2374A>C |
| NRCAM transcript variant 42 | NM_001371161.1:c.2431= | NM_001371161.1:c.2431A>C |
| NRCAM transcript variant 39 | NM_001371179.1:c.2113= | NM_001371179.1:c.2113A>C |
| NRCAM transcript variant 61 | NM_001371160.1:c.2413= | NM_001371160.1:c.2413A>C |
| NRCAM transcript variant 48 | NM_001371135.1:c.2374= | NM_001371135.1:c.2374A>C |
| NRCAM transcript variant 68 | NM_001371159.1:c.2401= | NM_001371159.1:c.2401A>C |
| NRCAM transcript variant 30 | NM_001371147.1:c.2086= | NM_001371147.1:c.2086A>C |
| NRCAM transcript variant 65 | NM_001371174.1:c.2401= | NM_001371174.1:c.2401A>C |
| NRCAM transcript variant 34 | NM_001371152.1:c.2383= | NM_001371152.1:c.2383A>C |
| NRCAM transcript variant 31 | NM_001371129.1:c.2374= | NM_001371129.1:c.2374A>C |
| NRCAM transcript variant 47 | NM_001371134.1:c.2380= | NM_001371134.1:c.2380A>C |
| NRCAM transcript variant 54 | NM_001371142.1:c.2086= | NM_001371142.1:c.2086A>C |
| NRCAM transcript variant 24 | NM_001371123.1:c.2431= | NM_001371123.1:c.2431A>C |
| NRCAM transcript variant 22 | NM_001371181.1:c.2374= | NM_001371181.1:c.2374A>C |
| NRCAM transcript variant 44 | NM_001371166.1:c.2374= | NM_001371166.1:c.2374A>C |
| NRCAM transcript variant 15 | NM_001371122.1:c.2374= | NM_001371122.1:c.2374A>C |
| NRCAM transcript variant 67 | NM_001371182.1:c.2326= | NM_001371182.1:c.2326A>C |
| NRCAM transcript variant 9 | NM_001371151.1:c.2383= | NM_001371151.1:c.2383A>C |
| NRCAM transcript variant 50 | NM_001371137.1:c.1474= | NM_001371137.1:c.1474A>C |
| NRCAM transcript variant 29 | NM_001371125.1:c.2086= | NM_001371125.1:c.2086A>C |
| NRCAM transcript variant 43 | NM_001371154.1:c.2374= | NM_001371154.1:c.2374A>C |
| NRCAM transcript variant 63 | NM_001371170.1:c.2113= | NM_001371170.1:c.2113A>C |
| NRCAM transcript variant 38 | NM_001371148.1:c.2113= | NM_001371148.1:c.2113A>C |
| NRCAM transcript variant 21 | NM_001371177.1:c.2374= | NM_001371177.1:c.2374A>C |
| NRCAM transcript variant 35 | NM_001371176.1:c.2383= | NM_001371176.1:c.2383A>C |
| NRCAM transcript variant 11 | NM_001371178.1:c.2383= | NM_001371178.1:c.2383A>C |
| NRCAM transcript variant 66 | NM_001371175.1:c.2383= | NM_001371175.1:c.2383A>C |
| NRCAM transcript variant 40 | NM_001371180.1:c.2113= | NM_001371180.1:c.2113A>C |
| NRCAM transcript variant X14 | XM_011516265.4:c.2431= | XM_011516265.4:c.2431A>C |
| NRCAM transcript variant X19 | XM_011516265.3:c.2431= | XM_011516265.3:c.2431A>C |
| NRCAM transcript variant X22 | XM_011516265.2:c.2431= | XM_011516265.2:c.2431A>C |
| NRCAM transcript variant X18 | XM_011516265.1:c.2431= | XM_011516265.1:c.2431A>C |
| NRCAM transcript variant X1 | XM_011516253.3:c.2431= | XM_011516253.3:c.2431A>C |
| NRCAM transcript variant X1 | XM_011516253.2:c.2431= | XM_011516253.2:c.2431A>C |
| NRCAM transcript variant X1 | XM_011516253.1:c.2431= | XM_011516253.1:c.2431A>C |
| NRCAM transcript variant X3 | XM_006716003.3:c.2431= | XM_006716003.3:c.2431A>C |
| NRCAM transcript variant X3 | XM_006716003.2:c.2431= | XM_006716003.2:c.2431A>C |
| NRCAM transcript variant X3 | XM_006716003.1:c.2431= | XM_006716003.1:c.2431A>C |
| NRCAM transcript variant X4 | XM_011516257.3:c.2413= | XM_011516257.3:c.2413A>C |
| NRCAM transcript variant X5 | XM_011516257.2:c.2413= | XM_011516257.2:c.2413A>C |
| NRCAM transcript variant X5 | XM_011516257.1:c.2413= | XM_011516257.1:c.2413A>C |
| NRCAM transcript variant X6 | XM_011516259.3:c.2401= | XM_011516259.3:c.2401A>C |
| NRCAM transcript variant X8 | XM_011516259.2:c.2401= | XM_011516259.2:c.2401A>C |
| NRCAM transcript variant X8 | XM_011516259.1:c.2401= | XM_011516259.1:c.2401A>C |
| NRCAM transcript variant X7 | XM_017012236.3:c.2401= | XM_017012236.3:c.2401A>C |
| NRCAM transcript variant X9 | XM_017012236.2:c.2401= | XM_017012236.2:c.2401A>C |
| NRCAM transcript variant X9 | XM_017012236.1:c.2401= | XM_017012236.1:c.2401A>C |
| NRCAM transcript variant X8 | XM_011516261.3:c.2383= | XM_011516261.3:c.2383A>C |
| NRCAM transcript variant X11 | XM_011516261.2:c.2383= | XM_011516261.2:c.2383A>C |
| NRCAM transcript variant X11 | XM_011516261.1:c.2383= | XM_011516261.1:c.2383A>C |
| NRCAM transcript variant X9 | XM_011516262.3:c.2374= | XM_011516262.3:c.2374A>C |
| NRCAM transcript variant X13 | XM_011516262.2:c.2374= | XM_011516262.2:c.2374A>C |
| NRCAM transcript variant X13 | XM_011516262.1:c.2374= | XM_011516262.1:c.2374A>C |
| NRCAM transcript variant X10 | XM_017012238.3:c.2374= | XM_017012238.3:c.2374A>C |
| NRCAM transcript variant X14 | XM_017012238.2:c.2374= | XM_017012238.2:c.2374A>C |
| NRCAM transcript variant X14 | XM_017012238.1:c.2374= | XM_017012238.1:c.2374A>C |
| NRCAM transcript variant X12 | XM_017012239.3:c.2356= | XM_017012239.3:c.2356A>C |
| NRCAM transcript variant X15 | XM_017012239.2:c.2356= | XM_017012239.2:c.2356A>C |
| NRCAM transcript variant X15 | XM_017012239.1:c.2356= | XM_017012239.1:c.2356A>C |
| NRCAM transcript variant X17 | XM_011516268.3:c.2143= | XM_011516268.3:c.2143A>C |
| NRCAM transcript variant X23 | XM_011516268.2:c.2143= | XM_011516268.2:c.2143A>C |
| NRCAM transcript variant X22 | XM_011516268.1:c.2143= | XM_011516268.1:c.2143A>C |
| NRCAM transcript variant X15 | XM_011516267.3:c.2431= | XM_011516267.3:c.2431A>C |
| NRCAM transcript variant X21 | XM_011516267.2:c.2431= | XM_011516267.2:c.2431A>C |
| NRCAM transcript variant X24 | XM_011516267.1:c.2431= | XM_011516267.1:c.2431A>C |
| NRCAM transcript variant X16 | XM_006716012.3:c.2431= | XM_006716012.3:c.2431A>C |
| NRCAM transcript variant X22 | XM_006716012.2:c.2431= | XM_006716012.2:c.2431A>C |
| NRCAM transcript variant X25 | XM_006716012.1:c.2431= | XM_006716012.1:c.2431A>C |
| NRCAM transcript variant X18 | XM_011516269.3:c.2431= | XM_011516269.3:c.2431A>C |
| NRCAM transcript variant X25 | XM_011516269.2:c.2431= | XM_011516269.2:c.2431A>C |
| NRCAM transcript variant X28 | XM_011516269.1:c.2431= | XM_011516269.1:c.2431A>C |
| NRCAM transcript variant X19 | XM_017012246.3:c.2401= | XM_017012246.3:c.2401A>C |
| NRCAM transcript variant X26 | XM_017012246.2:c.2401= | XM_017012246.2:c.2401A>C |
| NRCAM transcript variant X29 | XM_017012246.1:c.2401= | XM_017012246.1:c.2401A>C |
| NRCAM transcript variant X20 | XM_006716014.3:c.2431= | XM_006716014.3:c.2431A>C |
| NRCAM transcript variant X27 | XM_006716014.2:c.2431= | XM_006716014.2:c.2431A>C |
| NRCAM transcript variant X30 | XM_006716014.1:c.2431= | XM_006716014.1:c.2431A>C |
| NRCAM transcript variant X21 | XM_011516270.3:c.2431= | XM_011516270.3:c.2431A>C |
| NRCAM transcript variant X28 | XM_011516270.2:c.2431= | XM_011516270.2:c.2431A>C |
| NRCAM transcript variant X31 | XM_011516270.1:c.2431= | XM_011516270.1:c.2431A>C |
| NRCAM transcript variant X24 | XM_017012248.3:c.2401= | XM_017012248.3:c.2401A>C |
| NRCAM transcript variant X31 | XM_017012248.2:c.2401= | XM_017012248.2:c.2401A>C |
| NRCAM transcript variant X34 | XM_017012248.1:c.2401= | XM_017012248.1:c.2401A>C |
| NRCAM transcript variant X23 | XM_017012247.3:c.2374= | XM_017012247.3:c.2374A>C |
| NRCAM transcript variant X30 | XM_017012247.2:c.2374= | XM_017012247.2:c.2374A>C |
| NRCAM transcript variant X33 | XM_017012247.1:c.2374= | XM_017012247.1:c.2374A>C |
| NRCAM transcript variant X25 | XM_017012251.3:c.2401= | XM_017012251.3:c.2401A>C |
| NRCAM transcript variant X34 | XM_017012251.2:c.2401= | XM_017012251.2:c.2401A>C |
| NRCAM transcript variant X37 | XM_017012251.1:c.2401= | XM_017012251.1:c.2401A>C |
| NRCAM transcript variant X2 | XM_011516255.2:c.2431= | XM_011516255.2:c.2431A>C |
| NRCAM transcript variant X2 | XM_011516255.1:c.2431= | XM_011516255.1:c.2431A>C |
| NRCAM transcript variant X5 | XM_011516258.2:c.2413= | XM_011516258.2:c.2413A>C |
| NRCAM transcript variant X6 | XM_011516258.1:c.2413= | XM_011516258.1:c.2413A>C |
| NRCAM transcript variant X26 | XM_024446777.2:c.2413= | XM_024446777.2:c.2413A>C |
| NRCAM transcript variant X39 | XM_024446777.1:c.2413= | XM_024446777.1:c.2413A>C |
| NRCAM transcript variant X28 | XM_024446778.2:c.2383= | XM_024446778.2:c.2383A>C |
| NRCAM transcript variant X42 | XM_024446778.1:c.2383= | XM_024446778.1:c.2383A>C |
| NRCAM transcript variant X33 | XM_024446779.2:c.2326= | XM_024446779.2:c.2326A>C |
| NRCAM transcript variant X43 | XM_024446779.1:c.2326= | XM_024446779.1:c.2326A>C |
| NRCAM transcript variant X35 | XM_024446780.2:c.2431= | XM_024446780.2:c.2431A>C |
| NRCAM transcript variant X44 | XM_024446780.1:c.2431= | XM_024446780.1:c.2431A>C |
| NRCAM transcript variant X11 | XM_047420417.1:c.2383= | XM_047420417.1:c.2383A>C |
| NRCAM transcript variant X13 | XM_047420418.1:c.2344= | XM_047420418.1:c.2344A>C |
| NRCAM transcript variant X22 | XM_047420419.1:c.2401= | XM_047420419.1:c.2401A>C |
| NRCAM transcript variant X27 | XM_047420420.1:c.2374= | XM_047420420.1:c.2374A>C |
| NRCAM transcript variant X30 | XM_047420422.1:c.2326= | XM_047420422.1:c.2326A>C |
| NRCAM transcript variant X32 | XM_047420424.1:c.2356= | XM_047420424.1:c.2356A>C |
| NRCAM transcript variant X29 | XM_047420421.1:c.2344= | XM_047420421.1:c.2344A>C |
| NRCAM transcript variant X31 | XM_047420423.1:c.2344= | XM_047420423.1:c.2344A>C |
| NRCAM transcript variant X34 | XM_047420425.1:c.2326= | XM_047420425.1:c.2326A>C |
| neuronal cell adhesion molecule isoform B precursor | NP_005001.3:p.Thr795= | NP_005001.3:p.Thr795Pro |
| neuronal cell adhesion molecule isoform A precursor | NP_001032209.1:p.Thr811= | NP_001032209.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform D precursor | NP_001180511.1:p.Thr811= | NP_001180511.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform E precursor | NP_001180512.1:p.Thr792= | NP_001180512.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform F precursor | NP_001180513.1:p.Thr792= | NP_001180513.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform H precursor | NP_001358055.1:p.Thr792= | NP_001358055.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform E precursor | NP_001358092.1:p.Thr792= | NP_001358092.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform A precursor | NP_001358060.1:p.Thr811= | NP_001358060.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform cc precursor | NP_001358085.1:p.Thr811= | NP_001358085.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform D precursor | NP_001358073.1:p.Thr811= | NP_001358073.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform gg precursor | NP_001358098.1:p.Thr811= | NP_001358098.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform H precursor | NP_001358101.1:p.Thr792= | NP_001358101.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform aa precursor | NP_001358075.1:p.Thr792= | NP_001358075.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform B precursor | NP_001358062.1:p.Thr795= | NP_001358062.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform D precursor | NP_001358097.1:p.Thr811= | NP_001358097.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform N precursor | NP_001358082.1:p.Thr811= | NP_001358082.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform D precursor | NP_001358057.1:p.Thr811= | NP_001358057.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform V precursor | NP_001358067.1:p.Thr811= | NP_001358067.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform E precursor | NP_001358094.1:p.Thr792= | NP_001358094.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform E precursor | NP_001358068.1:p.Thr792= | NP_001358068.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform ee precursor | NP_001358087.1:p.Thr792= | NP_001358087.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform E precursor | NP_001358084.1:p.Thr792= | NP_001358084.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform P precursor | NP_001358048.1:p.Thr792= | NP_001358048.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform H precursor | NP_001358053.1:p.Thr792= | NP_001358053.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform Z precursor | NP_001358074.1:p.Thr792= | NP_001358074.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform E precursor | NP_001358096.1:p.Thr792= | NP_001358096.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform F precursor | NP_001358091.1:p.Thr792= | NP_001358091.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform T precursor | NP_001358065.1:p.Thr795= | NP_001358065.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform J precursor | NP_001358061.1:p.Thr792= | NP_001358061.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform W precursor | NP_001358069.1:p.Thr792= | NP_001358069.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform B precursor | NP_001358100.1:p.Thr795= | NP_001358100.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform L | NP_001358072.1:p.Thr696= | NP_001358072.1:p.Thr696Pro |
| neuronal cell adhesion molecule isoform G precursor | NP_001358078.1:p.Thr811= | NP_001358078.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform Q precursor | NP_001358056.1:p.Thr810= | NP_001358056.1:p.Thr810Pro |
| neuronal cell adhesion molecule isoform K precursor | NP_001358059.1:p.Thr795= | NP_001358059.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform bb precursor | NP_001358079.1:p.Thr801= | NP_001358079.1:p.Thr801Pro |
| neuronal cell adhesion molecule isoform L | NP_001358093.1:p.Thr696= | NP_001358093.1:p.Thr696Pro |
| neuronal cell adhesion molecule isoform ii precursor | NP_001358102.1:p.Thr811= | NP_001358102.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform dd precursor | NP_001358086.1:p.Thr795= | NP_001358086.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform X precursor | NP_001358070.1:p.Thr792= | NP_001358070.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform N precursor | NP_001358090.1:p.Thr811= | NP_001358090.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform M | NP_001358108.1:p.Thr705= | NP_001358108.1:p.Thr705Pro |
| neuronal cell adhesion molecule isoform ff precursor | NP_001358089.1:p.Thr805= | NP_001358089.1:p.Thr805Pro |
| neuronal cell adhesion molecule isoform S precursor | NP_001358064.1:p.Thr792= | NP_001358064.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform ll precursor | NP_001358088.1:p.Thr801= | NP_001358088.1:p.Thr801Pro |
| neuronal cell adhesion molecule isoform I | NP_001358076.1:p.Thr696= | NP_001358076.1:p.Thr696Pro |
| neuronal cell adhesion molecule isoform jj precursor | NP_001358103.1:p.Thr801= | NP_001358103.1:p.Thr801Pro |
| neuronal cell adhesion molecule isoform K precursor | NP_001358081.1:p.Thr795= | NP_001358081.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform J precursor | NP_001358058.1:p.Thr792= | NP_001358058.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform R precursor | NP_001358063.1:p.Thr794= | NP_001358063.1:p.Thr794Pro |
| neuronal cell adhesion molecule isoform Y | NP_001358071.1:p.Thr696= | NP_001358071.1:p.Thr696Pro |
| neuronal cell adhesion molecule isoform G precursor | NP_001358052.1:p.Thr811= | NP_001358052.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform E precursor | NP_001358110.1:p.Thr792= | NP_001358110.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform O precursor | NP_001358095.1:p.Thr792= | NP_001358095.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform E precursor | NP_001358051.1:p.Thr792= | NP_001358051.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform mm precursor | NP_001358111.1:p.Thr776= | NP_001358111.1:p.Thr776Pro |
| neuronal cell adhesion molecule isoform B precursor | NP_001358080.1:p.Thr795= | NP_001358080.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform U | NP_001358066.1:p.Thr492= | NP_001358066.1:p.Thr492Pro |
| neuronal cell adhesion molecule isoform I | NP_001358054.1:p.Thr696= | NP_001358054.1:p.Thr696Pro |
| neuronal cell adhesion molecule isoform O precursor | NP_001358083.1:p.Thr792= | NP_001358083.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform hh | NP_001358099.1:p.Thr705= | NP_001358099.1:p.Thr705Pro |
| neuronal cell adhesion molecule isoform M | NP_001358077.1:p.Thr705= | NP_001358077.1:p.Thr705Pro |
| neuronal cell adhesion molecule isoform E precursor | NP_001358106.1:p.Thr792= | NP_001358106.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform K precursor | NP_001358105.1:p.Thr795= | NP_001358105.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform B precursor | NP_001358107.1:p.Thr795= | NP_001358107.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform kk precursor | NP_001358104.1:p.Thr795= | NP_001358104.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform M | NP_001358109.1:p.Thr705= | NP_001358109.1:p.Thr705Pro |
| neuronal cell adhesion molecule isoform X12 | XP_011514567.1:p.Thr811= | XP_011514567.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform X1 | XP_011514555.1:p.Thr811= | XP_011514555.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform X2 | XP_006716066.1:p.Thr811= | XP_006716066.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform X3 | XP_011514559.1:p.Thr805= | XP_011514559.1:p.Thr805Pro |
| neuronal cell adhesion molecule isoform X4 | XP_011514561.1:p.Thr801= | XP_011514561.1:p.Thr801Pro |
| neuronal cell adhesion molecule isoform X5 | XP_016867725.1:p.Thr801= | XP_016867725.1:p.Thr801Pro |
| neuronal cell adhesion molecule isoform X6 | XP_011514563.1:p.Thr795= | XP_011514563.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform X7 | XP_011514564.1:p.Thr792= | XP_011514564.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform X8 | XP_016867727.1:p.Thr792= | XP_016867727.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform X10 | XP_016867728.1:p.Thr786= | XP_016867728.1:p.Thr786Pro |
| neuronal cell adhesion molecule isoform X15 | XP_011514570.1:p.Thr715= | XP_011514570.1:p.Thr715Pro |
| neuronal cell adhesion molecule isoform X13 | XP_011514569.1:p.Thr811= | XP_011514569.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform X14 | XP_006716075.1:p.Thr811= | XP_006716075.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform X16 | XP_011514571.1:p.Thr811= | XP_011514571.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform X17 | XP_016867735.1:p.Thr801= | XP_016867735.1:p.Thr801Pro |
| neuronal cell adhesion molecule isoform X18 | XP_006716077.1:p.Thr811= | XP_006716077.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform X19 | XP_011514572.1:p.Thr811= | XP_011514572.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform X22 | XP_016867737.1:p.Thr801= | XP_016867737.1:p.Thr801Pro |
| neuronal cell adhesion molecule isoform X21 | XP_016867736.1:p.Thr792= | XP_016867736.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform X23 | XP_016867740.1:p.Thr801= | XP_016867740.1:p.Thr801Pro |
| neuronal cell adhesion molecule isoform X1 | XP_011514557.1:p.Thr811= | XP_011514557.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform X3 | XP_011514560.1:p.Thr805= | XP_011514560.1:p.Thr805Pro |
| neuronal cell adhesion molecule isoform X24 | XP_024302545.1:p.Thr805= | XP_024302545.1:p.Thr805Pro |
| neuronal cell adhesion molecule isoform X26 | XP_024302546.1:p.Thr795= | XP_024302546.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform X31 | XP_024302547.1:p.Thr776= | XP_024302547.1:p.Thr776Pro |
| neuronal cell adhesion molecule isoform X33 | XP_024302548.1:p.Thr811= | XP_024302548.1:p.Thr811Pro |
| neuronal cell adhesion molecule isoform X9 | XP_047276373.1:p.Thr795= | XP_047276373.1:p.Thr795Pro |
| neuronal cell adhesion molecule isoform X11 | XP_047276374.1:p.Thr782= | XP_047276374.1:p.Thr782Pro |
| neuronal cell adhesion molecule isoform X20 | XP_047276375.1:p.Thr801= | XP_047276375.1:p.Thr801Pro |
| neuronal cell adhesion molecule isoform X25 | XP_047276376.1:p.Thr792= | XP_047276376.1:p.Thr792Pro |
| neuronal cell adhesion molecule isoform X28 | XP_047276378.1:p.Thr776= | XP_047276378.1:p.Thr776Pro |
| neuronal cell adhesion molecule isoform X30 | XP_047276380.1:p.Thr786= | XP_047276380.1:p.Thr786Pro |
| neuronal cell adhesion molecule isoform X27 | XP_047276377.1:p.Thr782= | XP_047276377.1:p.Thr782Pro |
| neuronal cell adhesion molecule isoform X29 | XP_047276379.1:p.Thr782= | XP_047276379.1:p.Thr782Pro |
| neuronal cell adhesion molecule isoform X32 | XP_047276381.1:p.Thr776= | XP_047276381.1:p.Thr776Pro |
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 | ss2736701666 | Nov 08, 2017 (151) |
| 2 | gnomAD - Exomes | NC_000007.13 - 107823238 | 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 rs1481119446
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.