Variant #0000276109 (NC_000011.9:g.31531348C>T, NM_019040.3:c.17C>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.31531348C>T
DNA change (hg38) g.31509801C>T
Published as ELP4(NM_001288726.1):c.17C>T (p.T6I), ELP4(NM_001288726.2):c.17C>T (p.T6I)
ISCN -
DB-ID ELP4_000001 See all 2 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) 2.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ELP4 NM_019040.3 -?/. - c.17C>T r.(?) p.(Thr6Ile)
IMMP1L NM_144981.1 -?/. - c.-375G>A r.(?) p.(=)
DNAJC24 NM_181706.4 -?/. - c.*79400C>T r.(=) p.(=)


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