Variant #0000344485 (NC_000004.11:g.169927999G>A, NM_016081.3:c.*80668G>A (PALLD))

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.169927999G>A
DNA change (hg38) g.169006848G>A
Published as -
ISCN -
DB-ID CBR4_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-16 16:34:40 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PALLD NM_016081.3 ?/. - c.*80668G>A r.(=) p.(=)
CBR4 NM_032783.4 ?/. - c.307C>T r.(?) p.(Gln103Ter)


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