Variant #0000279847 (NC_000001.10:g.45966071G>T, MMACHC(NM_015506.2):c.67G>T)

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45966071G>T
DNA change (hg38) g.45500399G>T
Published as MMACHC(NM_015506.2):c.67G>T (p.V23F)
ISCN -
DB-ID MMACHC_000003 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 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00041 View details
Owner VKGL-NL_AMC
Database submission license No license selected
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MMACHC NM_015506.2 ?/. - c.67G>T r.(?) p.(Val23Phe)
PRDX1 NM_181697.2 ?/. - c.*10930C>A r.(=) p.(=)