Variant #0000545384 (NC_000011.9:g.67258367C>T, NM_003977.2:c.896C>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.67258367C>T
DNA change (hg38) g.67490896C>T
Published as AIP(NM_001302959.1):c.719C>T (p.(Ala240Val)), AIP(NM_003977.2):c.896C>T (p.A299V)
ISCN -
DB-ID AIP_000013 See all 4 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIP NM_003977.2 ?/. - c.896C>T r.(?) p.(Ala299Val)
PITPNM1 NM_004910.2 ?/. - c.*1137G>A r.(=) p.(=)


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