Variant #0001044377 (NC_000023.10:g.49041069G>A, NM_003179.2:c.*4671C>T (SYP))

Chromosome X
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.49041069G>A
DNA change (hg38) -
Published as PRICKLE3(NM_006150.5):c.128+9C>T
ISCN -
DB-ID SYP_000032
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) 0.0019 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     
PLP2 NM_002668.2 -?/. - c.*10026G>A r.(=) p.(=)
SYP NM_003179.2 -?/. - c.*4671C>T r.(=) p.(=)
PRICKLE3 NM_006150.3 -?/. - c.128+9C>T r.(=) p.(=)


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