Variant #0000279853 (NC_000005.9:g.52398005T>C, NM_176806.3:c.*68A>G (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.52398005T>C
DNA change (hg38) g.53102175T>C
Published as MOCS2(NM_004531.5):c.148A>G (p.T50A)
ISCN -
DB-ID MOCS2_000008
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) 0.03885 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MOCS2 NM_004531.4 -/. - c.148A>G r.(?) p.(Thr50Ala)
MOCS2 NM_176806.3 -/. - c.*68A>G r.(=) p.(=)


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