Variant #0000305509 (NC_000017.10:g.4849268T>C, NM_003562.4:c.-6063A>G (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.4849268T>C
DNA change (hg38) g.4945973T>C
Published as PFN1(NM_005022.3):c.350A>G (p.E117G)
ISCN -
DB-ID PFN1_000002 See all 5 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) 0.0005 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 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENO3 NM_001193503.1 ?/. - c.-5212T>C r.(?) p.(=)
SLC25A11 NM_003562.4 ?/. - c.-6063A>G r.(?) p.(=)
PFN1 NM_005022.3 ?/. - c.350A>G r.(?) p.(Glu117Gly)
RNF167 NM_015528.1 ?/. - c.*957T>C r.(=) p.(=)


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