Variant #0000726507 (NC_000017.10:g.4856369A>C, NM_005022.3:c.-4680T>G (PFN1))

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.4856369A>C
DNA change (hg38) -
Published as ENO3(NM_001976.4):c.205A>C (p.I69L)
ISCN -
DB-ID ENO3_000009
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ENO3 NM_001193503.1 -?/. - c.181+184A>C r.(=) p.(=)
PFN1 NM_005022.3 -?/. - c.-4680T>G r.(?) p.(=)


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