Variant #0000803322 (NC_000007.13:g.98987597T>C, NM_014891.6:c.*6708A>G (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.98987597T>C
DNA change (hg38) -
Published as ARPC1B(NM_005720.4):c.462T>C (p.N154=)
ISCN -
DB-ID PDAP1_000009
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) 1.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
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.462T>C r.(?) p.(Asn154=)
PDAP1 NM_014891.6 -?/. - c.*6708A>G r.(=) p.(=)


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