Variant #0001065229 (NC_000010.10:g.64936106A>G, NM_004241.2:c.6641T>C (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.64936106A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID JMJD1C_000078
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
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.-345200A>G r.(?) p.(=)
JMJD1C NM_004241.2 ?/. - c.6641T>C r.(?) p.(Ile2214Thr)
JMJD1C NM_032776.1 ?/. - c.7352T>C r.(?) p.(Ile2451Thr)


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