Variant #0000860341 (NC_000006.11:g.39847207A>G, NM_005943.5:c.*27694T>C (MOCS1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.39847207A>G
DNA change (hg38) -
Published as DAAM2(NM_001201427.2):c.1799A>G (p.Q600R)
ISCN -
DB-ID DAAM2_000031
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) 0.00209 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DAAM2 NM_001201427.1 -?/. - c.1799A>G r.(?) p.(Gln600Arg)
MOCS1 NM_005943.5 -?/. - c.*27694T>C r.(=) p.(=)


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