Variant #0000249542 (NC_000006.11:g.39902170A>G, NM_005943.5:c.-6853T>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.39902170A>G
DNA change (hg38) g.39934431A>G
Published as MOCS1(NM_001075098.4):c.-14T>C
ISCN -
DB-ID MOCS1_000026
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) 0.0001 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.*32357A>G r.(=) p.(=)
MOCS1 NM_005943.5 -?/. - c.-6853T>C r.(?) p.(=)


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