Variant #0000283702 (NC_000006.11:g.39893421C>T, NC_000006.11(NM_005943.5):c.418+1G>A (MOCS1))

Chromosome 6
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.39893421C>T
DNA change (hg38) g.39925677C>T
Published as MOCS1(NM_001358530.2):c.418+1G>A, MOCS1(NM_005943.6):c.418+1G>A
ISCN -
DB-ID MOCS1_000007 See all 4 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) 4.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DAAM2 NM_001201427.1 +/. - c.*23608C>T r.(=) p.(=)
MOCS1 NM_005943.5 +/. - c.418+1G>A r.spl? p.?


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