Variant #0000623098 (NC_000014.8:g.105858069T>A, NM_001100913.2:c.2221T>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.105858069T>A
DNA change (hg38) g.105391732T>A
Published as PACS2(NM_001100913.3):c.2221T>A (p.S741T)
ISCN -
DB-ID BRF1_000020
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +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     
PACS2 NM_001100913.2 ?/. - c.2221T>A r.(?) p.(Ser741Thr)
BRF1 NM_001242786.1 ?/. - c.-76572A>T r.(?) p.(=)


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