Variant #0001015610 (NC_000017.10:g.67303085T>C, NM_172232.2:c.569A>G (ABCA5))

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.67303085T>C
DNA change (hg38) -
Published as ABCA5(NM_018672.5):c.569A>G (p.N190S)
ISCN -
DB-ID ABCA10_000004
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) 0.00059 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.-63008A>G r.(?) p.(=)
ABCA5 NM_172232.2 -?/. - c.569A>G r.(?) p.(Asn190Ser)


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