Variant #0000540189 (NC_000010.10:g.64973487G>A, NM_004241.2:c.1783C>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.64973487G>A
DNA change (hg38) g.63213727G>A
Published as -
ISCN -
DB-ID JMJD1C_000010
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +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.-307819G>A r.(?) p.(=)
JMJD1C NM_004241.2 ?/. - c.1783C>T r.(?) p.(Arg595Ter)
JMJD1C NM_032776.1 ?/. - c.2440C>T r.(?) p.(Arg814Ter)


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