Variant #0000533173 (NC_000007.13:g.98988511G>T, NM_014891.6:c.*5794C>A (PDAP1))

Chromosome 7
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.98988511G>T
DNA change (hg38) g.99390888G>T
Published as ARPC1B(NM_005720.3):c.501-5G>T (p.?), ARPC1B(NM_005720.4):c.501-5G>T
ISCN -
DB-ID ARPC1B_000001 See all 2 reported entries
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) 0.00278 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 10:37:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARPC1B NM_005720.3 -?/. - c.501-5G>T r.spl? p.?
PDAP1 NM_014891.6 -?/. - c.*5794C>A r.(=) p.(=)


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