Variant #0000258950 (NC_000001.10:g.150531050G>A, NM_019032.4:c.2484G>A (ADAMTSL4))

Chromosome 1
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.150531050G>A
DNA change (hg38) g.150558574G>A
Published as ADAMTSL4(NM_019032.4):c.2484G>A (p.P828P), ADAMTSL4(NM_019032.6):c.2484G>A (p.P828=)
ISCN -
DB-ID ADAMTSL4_000005 See all 8 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) 0.87055 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 2018-01-15 20:58:59 +01:00 (CET)
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     
ADAMTSL4 NM_019032.4 -/. - c.2484G>A r.(?) p.(Pro828=)


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