Variant #0000933294 (NC_000017.10:g.42332665_42332666delinsA, NC_000017.10(NM_000342.3):c.1801-2_1801-1delinsT (SLC4A1))

Chromosome 17
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.42332665_42332666delinsA
DNA change (hg38) -
Published as -
ISCN -
DB-ID SLC4A1_000083
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
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 2023-09-05 16:55:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC4A1 NM_000342.3 +/. - c.1801-2_1801-1delinsT r.(?) p.(?)


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