Variant #0000925166 (NC_000010.10:g.64949103T>A, NM_004241.2:c.5684A>T (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.64949103T>A
DNA change (hg38) -
Published as JMJD1C(NM_032776.3):c.6395A>T (p.K2132I)
ISCN -
DB-ID JMJD1C_000052
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) 0.00108 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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
REEP3 NM_001001330.2 ?/. - c.-332203T>A r.(?) p.(=)
JMJD1C NM_004241.2 ?/. - c.5684A>T r.(?) p.(Lys1895Ile)
JMJD1C NM_032776.1 ?/. - c.6395A>T r.(?) p.(Lys2132Ile)


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