Variant #0000622395 (NC_000010.10:g.64949097T>C, NM_004241.2:c.5690A>G (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.64949097T>C
DNA change (hg38) g.63189337T>C
Published as JMJD1C(NM_032776.3):c.6401A>G (p.E2134G)
ISCN -
DB-ID JMJD1C_000015
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) 1.0E-5 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 2019-12-06 12:43:26 +01:00 (CET)
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.-332209T>C r.(?) p.(=)
JMJD1C NM_004241.2 ?/. - c.5690A>G r.(?) p.(Glu1897Gly)
JMJD1C NM_032776.1 ?/. - c.6401A>G r.(?) p.(Glu2134Gly)


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