Variant #0000507717 (NC_000001.10:g.46088735A>G, NM_002482.3:c.*4922A>G (NASP))

Chromosome 1
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.46088735A>G
DNA change (hg38) g.45623063A>G
Published as CCDC17(NM_001114938.2):c.548T>C (p.(Leu183Pro))
ISCN -
DB-ID CCDC17_000003
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_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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC17 NM_001190182.1 -?/. - c.521T>C r.(?) p.(Leu174Pro)
NASP NM_002482.3 -?/. - c.*4922A>G r.(=) p.(=)
GPBP1L1 NM_021639.4 -?/. - c.*5193T>C r.(=) p.(=)


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