| RefSNP | | Organism: | human (Homo sapiens) | | Molecule Type: | Genomic | | Created/Updated in build: | 126/130 | | Map to Genome Build: | 36.3 |
| | Allele | | Variation Class: | DIP: deletion/insertion polymorphism | | RefSNP Alleles: | -/A | | Ancestral Allele: | Not available | | Clinical Association: | unknown |
| | HGVS Names | | NM_000550.2:c.1584_1585insA |
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SNP Details are organized in the following sections:
The submission ss43431270 has the longest flanking sequence of all cluster members and was used to instantiate sequence for rs34883117 during BLAST analysis for the current build.
NCBI Assay ID | Handle|Submitter ID | Validation Status | ss to rs Orientation /Strand | Alleles | 5' Near Seq 30 bp | 3' Near Seq 30 bp | Entry Date | Update Date | Build Added | Molecule Type | Freq Warning | Ancestral Allele | Success Rate |
|---|
| ss43431270 | ABI|hCV33355943 |       | fwd/ | -/A | tatcaatgctatgctgaagaatatgaaaaa | ctccagaatcctaatcagtctgtggtctaa | 07/18/05 | 07/18/05 | 126 | Genomic | | | unknown |
>gnl|dbSNP|rs34883117|allelePos=301|totalLen=601|taxid=9606|snpclass=2|alleles='-/A'|mol=Genomic|build=126 GCCAATGTAA ATTAAATATG AGGATTTCTG TTAAAATAGA CATTTCTAAA TTTCATGTGT
CCACTTTTTG GTGATAACTA TTTTAATATT TGTCTTTTTA TTTTTAATCT TCCTTTCCAA
ATAGGTCGGG AGTTTAGTGT ACCTGAGATA ATTGCCATAG CAGTAGTTGG CGCTTTGTTA
CTGGTTGCAC TCATTTTTGG GACTGCTTCT TATCTGATTC GTGCCAGACG CAGTATGGAT
GAAGCTAACC AGCCTCTCCT CACTGATCAG TATCAATGCT ATGCTGAAGA ATATGAAAAA
N
CTCCAGAATC CTAATCAGTC TGTGGTCTAA CAAATGCCCT ACTCTCTTAT GCATTAGTAT
CACAAAACCA CCTGGTTGAA TATAATAGAT TGAGTTATTA ACTGTATTTT CTTTCACTTT
ATTACCTTCT TTCTAATACA AGCATATGTT AGAATTAAAG TTCTAGGCAT ACTTTTCAAA
GCTGGGAAGA CCCTTTCAGA ATCTTTTCAA TGGGTTTTAA TTTTCAGTTC TATTTAAAAT
GGTGAATGAC ACTAAACTCC ATGATATTTA AGGATAGTGT GAAGATCTTT GGCATGATTT
GeneView via analysis of contig annotation:
View more variation on this gene (click to hide).
| Assembly |
SNP to Chr |
Chr |
Chr position |
Contig |
Contig position |
Allele |
| Function |
mRNA |
Protein |
| mRNA to Chr |
Accession |
Position |
Allele change |
Accession |
Position |
Residue change |
on assembly: is labeled at position on chromosome .
GeneView via analysis of contig annotation: N/A.
GeneView via direct blast against RefSeq sequences (used when no gene model is available):
| Function |
Chr |
mRNA |
Protein |
| SNP to mRNA |
Accession |
Position |
Allele change |
Accession |
Position |
Residue change |
on assembly: is labeled at position on chromosome .
GeneView via direct blast against RefSeq sequences (used when no gene model is available): N/A
doesn't map to any assembly.
There is no frequency data.
| Validation status | Marker displays Mendelian segregation | PCR results confirmed in multiple reactions | Homozygotes detected in individual genotype data |       | UNKNOWN | UNKNOWN | UNKNOWN |
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