Variant #0001045690 (NC_000001.10:g.45973876_45973881dup, NC_000001.10(NM_015506.2):c.277-8_277-3dup (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.45973876_45973881dup
DNA change (hg38) -
Published as MMACHC(NM_001330540.1):c.106-8_106-3dup (p.?)
ISCN -
DB-ID MMACHC_000065
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) Retrieve
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.277-8_277-3dup r.spl? p.?
PRDX1 NM_181697.2 -?/. - c.*3121_*3126dup r.(=) p.(=)


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