Variant #0000305508 (NC_000017.10:g.4849284G>A, NM_003562.4:c.-6079C>T (SLC25A11))

Chromosome 17
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.4849284G>A
DNA change (hg38) g.4945989G>A
Published as PFN1(NM_005022.3):c.334C>T (p.L112=), PFN1(NM_005022.4):c.334C>T (p.L112=)
ISCN -
DB-ID PFN1_000003 See all 4 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) 0.06976 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENO3 NM_001193503.1 -?/. - c.-5196G>A r.(?) p.(=)
SLC25A11 NM_003562.4 -?/. - c.-6079C>T r.(?) p.(=)
PFN1 NM_005022.3 -?/. - c.334C>T r.(?) p.(Leu112=)
RNF167 NM_015528.1 -?/. - c.*973G>A r.(=) p.(=)


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