Variant #0000998428 (NC_000010.10:g.64957320T>C, NM_004241.2:c.4838A>G (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.64957320T>C
DNA change (hg38) -
Published as JMJD1C(NM_032776.1):c.5495A>G (p.(Lys1832Arg))
ISCN -
DB-ID JMJD1C_000057
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.-323986T>C r.(?) p.(=)
JMJD1C NM_004241.2 ?/. - c.4838A>G r.(?) p.(Lys1613Arg)
JMJD1C NM_032776.1 ?/. - c.5495A>G r.(?) p.(Lys1832Arg)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.