Variant #0000976262 (NC_000004.11:g.2077246C>T, NM_181808.2:c.2388G>A (POLN))

Chromosome 4
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.2077246C>T
DNA change (hg38) -
Published as POLN(NM_181808.4):c.2388G>A (p.(Arg796=))
ISCN -
DB-ID HAUS3_000006
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) 0.00028 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 2024-04-19 20:27:30 +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     
HAUS3 NM_024511.5 ?/. - c.*156408G>A r.(=) p.(=)
POLN NM_181808.2 ?/. - c.2388G>A r.(?) p.(=)


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