Variant #0000004356 (NC_000005.9:g.70220952_70220953insA, SMN1(NM_000344.3):c.22_23insA)

Individual ID 00004356
Chromosome 5
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.70220952_70220953insA
Reference Zeng J1, Lin Y, Yan A, Ke L, Zhu Z, Lan F.(2011)
DB-ID SMN1_000020 See all 2 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 ./. 1 c.22_23insA r.(?) p.(Ser8Lysfs*23) VariO:0142 DNA insertion VariO:0023 amphigoric amino acid indel



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000004356 ? ? SMN1 1 Y Yang