Variant #0000001692 (NC_000014.8:g.103390126C>T, NM_030943.3:c.122C>T (AMN))

Chromosome 14
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.103390126C>T
DNA change (hg38) g.102923789C>T
Published as -
ISCN -
DB-ID AMN_000002
Variant remarks 1 Norwegian MGA1 family
Reference PubMed: Tanner et al. 2003
ClinVar ID -
dbSNP ID rs119478058
Origin SUMMARY record
Segregation yes
Frequency 0/177 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-09-07 08:42:38 +02:00 (CEST)
Date last edited 2017-05-05 19:04:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMN NM_030943.3 +/+ 02 c.122C>T r.122c>u p.Thr41Ile


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