Variant #0000262153 (NC_000017.10:g.6337427C>T, NC_000017.10(NM_014336.3):c.97-9G>A (AIPL1))

Chromosome 17
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.6337427C>T
DNA change (hg38) g.6434107C>T
Published as AIPL1(NM_014336.4):c.97-9G>A, AIPL1(NM_014336.5):c.97-9G>A
ISCN -
DB-ID AIPL1_000029 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) 0.00111 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 2018-01-15 20:58:59 +01:00 (CET)
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     
AIPL1 NM_014336.3 -?/. - c.97-9G>A r.(=) p.(=)


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