Variant #0000976805 (NC_000005.9:g.52397927C>T, NM_176806.3:c.*146G>A (MOCS2))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.52397927C>T
DNA change (hg38) -
Published as MOCS2(NM_004531.5):c.226G>A (p.(Gly76Arg))
ISCN -
DB-ID MOCS2_000033 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 -
Methylation -
Average frequency (gnomAD v.2.1.1) 5.0E-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 2024-04-19 20:27:30 +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     
MOCS2 NM_004531.4 +?/. - c.226G>A r.(?) p.(Gly76Arg)
MOCS2 NM_176806.3 +?/. - c.*146G>A r.(=) p.(=)


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