Variant #0001037937 (NC_000010.10:g.64950745C>T, NM_004241.2:c.5489G>A (JMJD1C))

Chromosome 10
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.64950745C>T
DNA change (hg38) -
Published as JMJD1C(NM_032776.3):c.6200G>A (p.(Arg2067Gln))
ISCN -
DB-ID JMJD1C_000074
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
REEP3 NM_001001330.2 ?/. - c.-330561C>T r.(?) p.(=)
JMJD1C NM_004241.2 ?/. - c.5489G>A r.(?) p.(Arg1830Gln)
JMJD1C NM_032776.1 ?/. - c.6200G>A r.(?) p.(Arg2067Gln)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.