Variant #0000852880 (NC_000011.9:g.31531432C>T, NM_019040.3:c.101C>T (ELP4))

Chromosome 11
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.31531432C>T
DNA change (hg38) -
Published as ELP4(NM_001288726.1):c.101C>T (p.P34L)
ISCN -
DB-ID DNAJC24_000003
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +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     
ELP4 NM_019040.3 -?/. - c.101C>T r.(?) p.(Pro34Leu)
IMMP1L NM_144981.1 -?/. - c.-459G>A r.(?) p.(=)
DNAJC24 NM_181706.4 -?/. - c.*79484C>T r.(=) p.(=)


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