Variant #0000004362 (NC_000005.9:g.70220935C>T, SMN1(NM_000344.3):c.5C>T)
Individual ID |
00004362 |
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.70220935C>T |
Reference |
Yamamoto T1, Sato H2, Lai PS3, Nurputra DK2, Harahap NI2, Morikawa S1, Nishimura N1, Kurashige T4, Ohshita T4, Nakajima H5, Yamada H6, Nishida Y6,(2014) |
DB-ID |
SMN1_000023 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Y Yang |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Y Yang |
Variant on transcripts
Screenings
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