Variant #0000605809 (NC_000001.10:g.46089267G>T, NM_002482.3:c.*5454G>T (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.46089267G>T
DNA change (hg38) g.45623595G>T
Published as CCDC17(NM_001114938.2):c.232C>A (p.(Gln78Lys))
ISCN -
DB-ID CCDC17_000005
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +01:00 (CET)
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.232C>A r.(?) p.(Gln78Lys)
NASP NM_002482.3 ?/. - c.*5454G>T r.(=) p.(=)
GPBP1L1 NM_021639.4 ?/. - c.*4661C>A r.(=) p.(=)


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