Variant #0001000943 (NC_000014.8:g.24551907G>A, NM_006177.3:c.151C>T (NRL))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.24551907G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID NRL_000017 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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     
PCK2 NM_001018073.1 +/. - c.-11708G>A r.(?) p.(=)
DCAF11 NM_001163484.1 +/. - c.-32279G>A r.(?) p.(=)
NRL NM_006177.3 +/. - c.151C>T r.(?) p.(Pro51Ser)


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