Variant #0000266548 (NC_000014.8:g.91780445G>A, NM_001080414.3:c.1715C>T (CCDC88C))

Chromosome 14
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.91780445G>A
DNA change (hg38) g.91314101G>A
Published as CCDC88C(NM_001080414.3):c.1715C>T (p.S572L, p.(Ser572Leu)), CCDC88C(NM_001080414.4):c.1715C>T (p.S572L)
ISCN -
DB-ID CCDC88C_000035 See all 3 reported entries
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) 0.00035 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC88C NM_001080414.3 -?/. - c.1715C>T r.(?) p.(Ser572Leu)


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