Variant #0001045070 (NC_000007.13:g.75932145C>T, NM_001540.3:c.116C>T (HSPB1))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.75932145C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID HSPB1_000018 See all 12 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs557327165
Origin Unknown
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 2025-05-28 11:08:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSPB1 NM_001540.3 +/. - c.116C>T r.(?) p.(Pro39Leu)


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