Variant #0000004366 (NC_000005.9:g.70240519C>T, SMN1(NM_000344.3):c.662C>T)

Individual ID 00004366
Chromosome 5
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.70240519C>T
Reference Kirwin SM1, Vinette KM1, Gonzalez IL1, Abdulwahed HA2, Al-Sannaa N2, Funanage VL1.(2013)
DB-ID SMN1_000026
Frequency -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
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.662C>T r.(?) p.(Pro221Leu) 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     
0000004366 ? ? SMN1 1 Y Yang