Variant #0000528802 (NC_000006.11:g.39877666G>A, NM_005943.5:c.1015C>T (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.39877666G>A
DNA change (hg38) g.39909922G>A
Published as MOCS1(NM_005943.5):c.1015C>T (p.R339W)
ISCN -
DB-ID MOCS1_000017
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) 0.00046 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-11-30 17:53:22 +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.*7853G>A r.(=) p.(=)
MOCS1 NM_005943.5 -?/. - c.1015C>T r.(?) p.(Arg339Trp)


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