Variant #0000528806 (NC_000006.11:g.39883802A>T, NC_000006.11(NM_005943.5):c.583+10T>A (MOCS1))

Chromosome 6
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.39883802A>T
DNA change (hg38) g.39916058A>T
Published as MOCS1(NM_005943.6):c.583+10T>A
ISCN -
DB-ID MOCS1_000021
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) 0.06842 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
DAAM2 NM_001201427.1 -/. - c.*13989A>T r.(=) p.(=)
MOCS1 NM_005943.5 -/. - c.583+10T>A r.(=) p.(=)


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