Variant #0001000617 (NC_000013.10:g.53216673C>T, NM_001011724.1:c.46C>T (HNRNPA1L2))

Chromosome 13
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.53216673C>T
DNA change (hg38) -
Published as HNRNPA1L2(NM_001011724.1):c.46C>T (p.(Leu16Phe))
ISCN -
DB-ID HNRNPA1L2_000004
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) 0.00024 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPA1L2 NM_001011724.1 ?/. - c.46C>T r.(?) p.(Leu16Phe)


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