Variant #0001003404 (NC_000017.10:g.4848185_4848186del, NM_003562.4:c.-4980_-4979del (SLC25A11))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.4848185_4848186del
DNA change (hg38) -
Published as RNF167(NM_015528.1):c.927_928delAC (p.(Leu310fs))
ISCN -
DB-ID PFN1_000015
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A11 NM_003562.4 ?/. - c.-4980_-4979del r.(?) p.(=)
PFN1 NM_005022.3 ?/. - c.*1010_*1011del r.(=) p.(=)
RNF167 NM_015528.1 ?/. - c.927_928del r.(?) p.(Leu310Phefs*4)


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