Variant #0000839897 (NC_000002.11:g.179318200G>C, NM_001042702.3:c.64G>C (DFNB59))

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.179318200G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID DFNB59_000056
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1214018581
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-02-15 18:32:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DFNB59 NM_001042702.3 ?/. - c.64G>C r.(?) p.(Val22Leu)


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