Variant #0000507718 (NC_000001.10:g.46089285G>A, NM_002482.3:c.*5472G>A (NASP))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.46089285G>A
DNA change (hg38) g.45623613G>A
Published as CCDC17(NM_001114938.2):c.214C>T (p.(Gln72Ter))
ISCN -
DB-ID CCDC17_000004
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) 0.00022 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC17 NM_001190182.1 ?/. - c.214C>T r.(?) p.(Gln72Ter)
NASP NM_002482.3 ?/. - c.*5472G>A r.(=) p.(=)
GPBP1L1 NM_021639.4 ?/. - c.*4643C>T r.(=) p.(=)


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