Variant #0000883481 (NC_000001.10:g.45973880C>G, NC_000001.10(NM_015506.2):c.277-4C>G (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.45973880C>G
DNA change (hg38) -
Published as MMACHC(NM_001330540.1):c.106-4C>G (p.?)
ISCN -
DB-ID MMACHC_000051
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) 0.00032 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +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.277-4C>G r.spl? p.?
PRDX1 NM_181697.2 -?/. - c.*3121G>C r.(=) p.(=)


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