Variant #0000004378 (NC_000005.9:g.70240546C>T, SMN1(NM_000344.3):c.689C>T)

Individual ID 00004378
Chromosome 5
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.70240546C>T
Reference DU J1, Qu YJ, Xiong H, Li EZ, Jin YW, Bai JL, Wang H, Song F.(2011)
DB-ID SMN1_000018 See all 5 reported entries
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 ./. 6 c.689C>T r.(?) p.(Ser230Leu) 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     
0000004378 ? ? SMN1 1 Y Yang