Variant #0000331007 (NC_000006.11:g.39880751G>A, NC_000006.11(NM_005943.5):c.758-3C>T (MOCS1))

Chromosome 6
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.39880751G>A
DNA change (hg38) g.39913007G>A
Published as MOCS1(NM_001075098.3):c.758-3C>T (p.?)
ISCN -
DB-ID MOCS1_000003
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) 0.00013 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DAAM2 NM_001201427.1 ?/. - c.*10938G>A r.(=) p.(=)
MOCS1 NM_005943.5 ?/. - c.758-3C>T r.spl? p.?


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