Variant #0000001697 (NC_000014.8:g.103395796_103395843del, NM_030943.3:c.683_730del (AMN))

Chromosome 14
Allele Unknown
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.103395796_103395843del
DNA change (hg38) g.102929459_102929506del
Published as -
ISCN -
DB-ID AMN_000006
Variant remarks 1 American MGA1 family
Reference PubMed: Tanner et al. 2004
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 09:14:41 +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 +/+ 07 c.683_730del r.(683_730del) p.(Gln228_Leu243del)


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