Variant #0001004833 (NC_000019.9:g.42806407C>T, NM_002573.3:c.55G>A (PAFAH1B3))

Chromosome 19
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.42806407C>T
DNA change (hg38) -
Published as PAFAH1B3(NM_002573.3):c.55G>A (p.(Gly19Ser))
ISCN -
DB-ID PAFAH1B3_000002
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) 0.00016 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 2024-08-28 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     
PAFAH1B3 NM_002573.3 ?/. - c.55G>A r.(?) p.(Gly19Ser)
PRR19 NM_199285.2 ?/. - c.-255C>T r.(?) p.(=)


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