Variant #0000001721 (NC_000014.8:g.103396840C>T, NC_000014.8(NM_030943.3):c.1257+10C>T (AMN))

Chromosome 14
Allele Both (homozygous)
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.103396840C>T
DNA change (hg38) g.102930503C>T
Published as -
ISCN -
DB-ID AMN_000022
Variant remarks 1 Maroccan MGA1 patient
Reference PubMed: Tanner et al. 2012
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
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 2012-09-10 14:39:38 +02:00 (CEST)
Date last edited 2020-07-06 09:08:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMN NM_030943.3 +?/+? i11 c.1257+10C>T r.spl? p.(=)


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