Variant #0000554341 (NC_000015.9:g.44066789C>T, NC_000015.9(NM_025165.2):c.823+5G>A (ELL3))

Chromosome 15
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.44066789C>T
DNA change (hg38) g.43774591C>T
Published as ELL3(NM_025165.2):c.823+5G>A (p.?)
ISCN -
DB-ID ELL3_000002
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) 0.00167 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-06 13:25:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERF2 NM_001199877.1 -?/. - c.-3438C>T r.(?) p.(=)
SERINC4 NM_001258031.1 -?/. - c.*20409G>A r.(=) p.(=)
PDIA3 NM_005313.4 -?/. - c.*3373C>T r.(=) p.(=)
ELL3 NM_025165.2 -?/. - c.823+5G>A r.spl? p.?


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