Variant #0000805331 (NC_000011.9:g.67258278C>T, NM_003977.2:c.807C>T (AIP))

Chromosome 11
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.67258278C>T
DNA change (hg38) -
Published as AIP(NM_001302960.1):c.799C>T (p.Q267*), AIP(NM_003977.4):c.807C>T (p.F269=)
ISCN -
DB-ID AIP_000011 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00057 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIP NM_003977.2 ?/. - c.807C>T r.(?) p.(Phe269=)
PITPNM1 NM_004910.2 ?/. - c.*1226G>A r.(=) p.(=)


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