Variant #0000614754 (NC_000014.8:g.105818730C>A, NM_001100913.2:c.223C>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.105818730C>A
DNA change (hg38) g.105352393C>A
Published as PACS2(NM_001100913.2):c.223C>A (p.L75M)
ISCN -
DB-ID BRF1_000017
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PACS2 NM_001100913.2 ?/. - c.223C>A r.(?) p.(Leu75Met)
BRF1 NM_001242786.1 ?/. - c.-37233G>T r.(?) p.(=)


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