Variant #0000261127 (NC_000001.10:g.197060077T>G, NM_018136.4:c.9539A>C (ASPM))

Chromosome 1
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.197060077T>G
DNA change (hg38) g.197090947T>G
Published as ASPM(NM_001206846.1):c.4784A>C (p.(Gln1595Pro)), ASPM(NM_018136.5):c.9539A>C (p.Q3180P)
ISCN -
DB-ID ASPM_000050 See all 9 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) 0.00478 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ASPM NM_018136.4 -?/. - c.9539A>C r.(?) p.(Gln3180Pro)


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