Variant #0000272157 (NC_000014.8:g.105688199G>A, NM_001100913.2:c.-93057G>A (PACS2))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.105688199G>A
DNA change (hg38) g.105221862G>A
Published as BRF1(NM_001519.4):c.1101C>T (p.D367=)
ISCN -
DB-ID BRF1_000003
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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-06 09:14:47 +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.-93057G>A r.(?) p.(=)
BRF1 NM_001242786.1 -?/. - c.756C>T r.(?) p.(Asp252=)
BTBD6 NM_033271.2 -?/. - c.-26788G>A r.(?) p.(=)


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