Variant #0000848757 (NC_000001.10:g.45974622G>C, NM_015506.2:c.584G>C (MMACHC))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45974622G>C
DNA change (hg38) -
Published as MMACHC(NM_001330540.1):c.413G>C (p.(Gly138Ala)), MMACHC(NM_015506.2):c.584G>C (p.G195A)
ISCN -
DB-ID MMACHC_000045 See all 2 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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MMACHC NM_015506.2 -?/. - c.584G>C r.(?) p.(Gly195Ala)
PRDX1 NM_181697.2 -?/. - c.*2379C>G r.(=) p.(=)


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