Variant #0000974008 (NC_000001.10:g.45973217dup, NM_015506.2:c.271dup (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.45973217dup
DNA change (hg38) -
Published as MMACHC(NM_001330540.1):c.100dup (p.(Arg34LysfsTer14)), MMACHC(NM_001330540.1):c.100dupA (p.R34Kfs*14), MMACHC(NM_001330540.2):c.100dupA (p.R34Kfs*...)
ISCN -
DB-ID MMACHC_000001 See all 5 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +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.271dup r.(?) p.(Arg91LysfsTer14)
PRDX1 NM_181697.2 +/. - c.*3784dup r.(?) p.(=)


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