Variant #0000961075 (NC_000001.10:g.45973995T>C, NM_015506.2:c.388T>C (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.45973995T>C
DNA change (hg38) -
Published as MMACHC(NM_015506.2):c.388T>C (p.(Tyr130His))
ISCN -
DB-ID MMACHC_000056
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) 2.0E-5 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 2024-02-26 20:06:56 +01:00 (CET)
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.388T>C r.(?) p.(Tyr130His)
PRDX1 NM_181697.2 +/. - c.*3006A>G r.(=) p.(=)


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