Variant #0000510088 (NC_000002.11:g.169728081_169728083del, NC_000002.11(NM_020675.3):c.551-7_551-5del (SPC25))

Chromosome 2
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.169728081_169728083del
DNA change (hg38) g.168871571_168871573del
Published as SPC25(NM_020675.3):c.551-8_551-6del (p.(=))
ISCN -
DB-ID SPC25_000001
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPC25 NM_020675.3 ?/. - c.551-7_551-5del r.spl? p.?


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