Variant #0001027540 (NC_000023.10:g.99922289A>G, NM_014467.2:c.980A>G (SRPX2))

Chromosome X
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.99922289A>G
DNA change (hg38) -
Published as SRPX2(NM_014467.2):c.980A>G (p.N327S, p.(Asn327Ser)), SRPX2(NM_014467.3):c.980A>G (p.N327S)
ISCN -
DB-ID SRPX2_000018 See all 6 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) 0.00058 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2025-02-07 18:57:27 +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     
SRPX2 NM_014467.2 ?/. - c.980A>G r.(?) p.(Asn327Ser)


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