Variant #0000720930 (NC_000006.11:g.39895101G>A, NM_005943.5:c.217C>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.39895101G>A
DNA change (hg38) -
Published as MOCS1(NM_001358530.2):c.217C>T (p.(Arg73Trp)), MOCS1(NM_005943.5):c.217C>T (p.R73W)
ISCN -
DB-ID DAAM2_000024 See all 2 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) 7.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DAAM2 NM_001201427.1 ?/. - c.*25288G>A r.(=) p.(=)
MOCS1 NM_005943.5 ?/. - c.217C>T r.(?) p.(Arg73Trp)


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