Variant #0000300602 (NC_000004.11:g.169815754G>A, NM_016081.3:c.2125G>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.169815754G>A
DNA change (hg38) g.168894603G>A
Published as PALLD(NM_001166108.2):c.2125G>A (p.A709T)
ISCN -
DB-ID PALLD_000010
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) 1.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PALLD NM_016081.3 ?/. - c.2125G>A r.(?) p.(Ala709Thr)
CBR4 NM_032783.4 ?/. - c.*95547C>T r.(=) p.(=)


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