Variant #0001045691 (NC_000001.10:g.45974520G>A, NM_015506.2:c.482G>A (MMACHC))

Chromosome 1
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.45974520G>A
DNA change (hg38) -
Published as MMACHC(NM_001330540.1):c.311G>A (p.(Arg104Gln))
ISCN -
DB-ID MMACHC_000066
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) 0.00016 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MMACHC NM_015506.2 +/. - c.482G>A r.(?) p.(Arg161Gln)
PRDX1 NM_181697.2 +/. - c.*2481C>T r.(=) p.(=)


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