Variant #0000341936 (NC_000004.11:g.146560724C>T, NM_172250.2:c.433C>T (MMAA))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.146560724C>T
DNA change (hg38) g.145639572C>T
Published as MMAA(NM_001375644.1):c.433C>T (p.R145*), MMAA(NM_172250.3):c.433C>T (p.R145*, p.(Arg145Ter))
ISCN -
DB-ID MMAA_000003 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00014 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MMAA NM_172250.2 +/. - c.433C>T r.(?) p.(Arg145Ter)


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