Variant #0000540181 (NC_000010.10:g.64927837C>T, NM_004241.2:c.6880G>A (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.64927837C>T
DNA change (hg38) g.63168077C>T
Published as JMJD1C(NM_032776.2):c.7591G>A (p.E2531K), JMJD1C(NM_032776.3):c.7591G>A (p.E2531K)
ISCN -
DB-ID JMJD1C_000003 See all 3 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) 0.00414 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
REEP3 NM_001001330.2 -?/. - c.-353469C>T r.(?) p.(=)
JMJD1C NM_004241.2 -?/. - c.6880G>A r.(?) p.(Glu2294Lys)
JMJD1C NM_032776.1 -?/. - c.7591G>A r.(?) p.(Glu2531Lys)


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