Variant #0000545386 (NC_000011.9:g.67258391A>G, NM_003977.2:c.920A>G (AIP))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.67258391A>G
DNA change (hg38) g.67490920A>G
Published as AIP(NM_003977.2):c.920A>G (p.Q307R), AIP(NM_003977.4):c.920A>G (p.Q307R)
ISCN -
DB-ID AIP_000019 See all 2 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) 0.99991 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIP NM_003977.2 -/. - c.920A>G r.(?) p.(Gln307Arg)
PITPNM1 NM_004910.2 -/. - c.*1113T>C r.(=) p.(=)


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