Variant #0000251012 (NC_000004.11:g.169819835A>G, NM_016081.3:c.2391A>G (PALLD))

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.169819835A>G
DNA change (hg38) g.168898684A>G
Published as PALLD(NM_001166108.2):c.2442A>G (p.T814=)
ISCN -
DB-ID PALLD_000011 See all 2 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) 0.00215 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.2391A>G r.(?) p.(Thr797=)
CBR4 NM_032783.4 -/. - c.*91466T>C r.(=) p.(=)


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