Variant #0001049080 (NC_000011.9:g.67258362C>A, NM_003977.2:c.891C>A (AIP))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.67258362C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID AIP_000027
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs35665586
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00133 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-10-10 16:41:02 +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     
AIP NM_003977.2 -?/. - c.891C>A r.(?) p.(Ala297=)


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