Variant #0001015609 (NC_000017.10:g.67299000_67299001del, NM_172232.2:c.977_978del (ABCA5))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.67299000_67299001del
DNA change (hg38) -
Published as ABCA5(NM_018672.5):c.977_978delAT (p.H326Rfs*5)
ISCN -
DB-ID ABCA5_000011 See all 5 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) 0.00017 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 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA10 NM_080282.3 +?/. - c.-58924_-58923del r.(?) p.(=)
ABCA5 NM_172232.2 +?/. - c.977_978del r.(?) p.(His326Argfs*5)


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