Variant #0000861936 (NC_000010.10:g.64967143G>A, NM_004241.2:c.3629C>T (JMJD1C))

Chromosome 10
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.64967143G>A
DNA change (hg38) -
Published as JMJD1C(NM_032776.2):c.4286C>T (p.S1429L), JMJD1C(NM_032776.3):c.4286C>T (p.S1429L)
ISCN -
DB-ID JMJD1C_000044 See all 2 reported entries
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) 0.00048 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
REEP3 NM_001001330.2 -?/. - c.-314163G>A r.(?) p.(=)
JMJD1C NM_004241.2 -?/. - c.3629C>T r.(?) p.(Ser1210Leu)
JMJD1C NM_032776.1 -?/. - c.4286C>T r.(?) p.(Ser1429Leu)


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