Variant #0000623095 (NC_000014.8:g.105683992G>C, NM_001100913.2:c.-97264G>C (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.105683992G>C
DNA change (hg38) g.105217655G>C
Published as BRF1(NM_001519.4):c.1661C>G (p.P554R)
ISCN -
DB-ID BRF1_000015
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) 2.0E-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 2019-12-06 12:43:26 +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.-97264G>C r.(?) p.(=)
BRF1 NM_001242786.1 -?/. - c.1382C>G r.(?) p.(Pro461Arg)
BTBD6 NM_033271.2 -?/. - c.-30995G>C r.(?) p.(=)


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