IMS-JST112657 |
JSNP ID |
IMS-JST112657 |
Chromosome |
12 |
Location |
12p13 |
Evidence of Location |
EntrezGene ID 3822 |
In Gene |
intron*3 |
Type |
SNP |
Frequencies |
0.500 |
allele |
C/A |
dbSNP ss# |
4945299 |
dbSNP rs# |
3759267 |
HGVBase-ID |
SNP002270724 |
5' assay |
GTAAGTACTGGCTGTGATGCACCTGAGGTAAAGTTGATATAGACGAAAATCAAGGTAGAA |
3' assay |
TTTATTCACGTGAATAATTCAAGGTGAAAAACGAGCCAAAATATAAACTATGTTTAAGGA |
Mapping Accession |
NT_009714.17;NT_009714.17 |
Mapping Position |
3334883;3350307 |
Mapping Symbol |
KLRC3 NKG2-E;KLRC2 NKG2-E |
Mapping OMIM-ID |
602892;602891 |
Screened Accession |
NT_009701.1 |
Screened Position |
962842 |
Screened Symbol |
KLRC2 |
Screened OMIM-ID |
- |