Variant #0000995089 (NC_000005.9:g.52397199G>A, NM_176806.3:c.*287C>T (MOCS2))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.52397199G>A
DNA change (hg38) -
Published as MOCS2(NM_004531.5):c.367C>T (p.H123Y)
ISCN -
DB-ID MOCS2_000002 See all 3 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) 0.00363 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-08-28 13:16:32 +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.367C>T r.(?) p.(His123Tyr)
MOCS2 NM_176806.3 -/. - c.*287C>T r.(=) p.(=)


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