Variant #0000964732 (NC_000007.13:g.98987580G>T, NM_014891.6:c.*6725C>A (PDAP1))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.98987580G>T
DNA change (hg38) -
Published as ARPC1B(NM_005720.4):c.445G>T (p.D149Y)
ISCN -
DB-ID PDAP1_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) 0.00078 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARPC1B NM_005720.3 -/. - c.445G>T r.(?) p.(Asp149Tyr)
PDAP1 NM_014891.6 -/. - c.*6725C>A r.(=) p.(=)


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