Variant #0000554346 (NC_000015.9:g.44089361C>T, NM_025165.2:c.-20262G>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.44089361C>T
DNA change (hg38) g.43797163C>T
Published as SERINC4(NM_001258031.1):c.826G>A (p.A276T)
ISCN -
DB-ID ELL3_000007
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) 3.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERF2 NM_001199877.1 -?/. - c.*3390C>T r.(=) p.(=)
SERINC4 NM_001258031.1 -?/. - c.826G>A r.(?) p.(Ala276Thr)
HYPK NM_016400.3 -?/. - c.-3436C>T r.(?) p.(=)
ELL3 NM_025165.2 -?/. - c.-20262G>A r.(?) p.(=)


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