Variant #0001031572 (NC_000001.10:g.197112670G>A, NM_018136.4:c.712C>T (ASPM))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.197112670G>A
DNA change (hg38) -
Published as ASPM(NM_018136.4):c.712C>T (p.P238S), ASPM(NM_018136.5):c.712C>T (p.(Pro238Ser))
ISCN -
DB-ID ASPM_000213 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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASPM NM_018136.4 ?/. - c.712C>T r.(?) p.(Pro238Ser)


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