Variant #0000863483 (NC_000014.8:g.105716323G>A, NM_001100913.2:c.-64933G>A (PACS2))

Chromosome 14
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.105716323G>A
DNA change (hg38) -
Published as BTBD6(NM_033271.2):c.772G>A (p.A258T)
ISCN -
DB-ID BRF1_000025
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +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     
PACS2 NM_001100913.2 ?/. - c.-64933G>A r.(?) p.(=)
BRF1 NM_001242786.1 ?/. - c.199+2521C>T r.(=) p.(=)
BTBD6 NM_033271.2 ?/. - c.772G>A r.(?) p.(Ala258Thr)


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