Variant #0000960290 (NC_000007.13:g.73457041G>C, NC_000007.13(NM_000501.2):c.325+5G>C (ELN))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.73457041G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID ELN_000189
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1791519372
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-02-22 17:56:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ELN NM_000501.2 +?/. - c.325+5G>C r.(?) p.(?)


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