Variant #0000889178 (NC_000010.10:g.64974659_64974661del, NM_004241.2:c.611_613del (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.64974659_64974661del
DNA change (hg38) -
Published as JMJD1C(NM_032776.3):c.1268_1270delGAG (p.G423del)
ISCN -
DB-ID JMJD1C_000050
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
REEP3 NM_001001330.2 ?/. - c.-306647_-306645del r.(?) p.(=)
JMJD1C NM_004241.2 ?/. - c.611_613del r.(?) p.(Gly204del)
JMJD1C NM_032776.1 ?/. - c.1268_1270del r.(?) p.(Gly423del)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.