Variant #0000998426 (NC_000010.10:g.64946031C>T, NM_004241.2:c.5972G>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.64946031C>T
DNA change (hg38) -
Published as JMJD1C(NM_032776.1):c.6683G>A (p.(Ser2228Asn))
ISCN -
DB-ID JMJD1C_000055
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.-335275C>T r.(?) p.(=)
JMJD1C NM_004241.2 -?/. - c.5972G>A r.(?) p.(Ser1991Asn)
JMJD1C NM_032776.1 -?/. - c.6683G>A r.(?) p.(Ser2228Asn)


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