Variant #0000979916 (NC_000011.9:g.793526C>T, NC_000011.9(NM_001191060.1):c.293+3G>A (SLC25A22))

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.793526C>T
DNA change (hg38) -
Published as SLC25A22(NM_001191061.2):c.293+3G>A
ISCN -
DB-ID CEND1_000013
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A22 NM_001191060.1 -?/. - c.293+3G>A r.spl? p.?
CEND1 NM_016564.3 -?/. - c.-3579G>A r.(?) p.(=)
PIDD NM_145886.3 -?/. - c.*5781G>A r.(=) p.(=)


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