Variant #0000276405 (NC_000001.10:g.6509033_6509044del, NM_031475.2:c.1797_1808del (ESPN))

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.6509033_6509044del
DNA change (hg38) g.6448973_6448984del
Published as ESPN(NM_031475.3):c.1797_1808delCCCACCGCCGCC (p.P602_P605del)
ISCN -
DB-ID ESPN_000006
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +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     
ESPN NM_031475.2 ?/. - c.1797_1808del r.(?) p.(Pro602_Pro605del)


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