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 InternationalCreative Commons License
Created by Y Yang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
SMN1 NM_000344.3 ./. 1 c.5C>T r.(?) p.(Ala2Val) VariO:0136 DNA substitution; VariO:0313 transition; VariO:0314 pyrimidine transition VariO:0021 amino acid substitution



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000004362 ? ? SMN1 1 Y Yang