Variant #0000951804 (NC_000023.10:g.99662827C>G, NM_001184880.1:c.769G>C (PCDH19))

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.99662827C>G
DNA change (hg38) -
Published as PCDH19(NM_001184880.1):c.769G>C (p.V257L), PCDH19(NM_001184880.2):c.769G>C (p.V257L)
ISCN -
DB-ID PCDH19_000124 See all 5 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) 0.00057 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 2023-11-27 17:35:39 +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     
PCDH19 NM_001184880.1 -?/. - c.769G>C r.(?) p.(Val257Leu)
PCDH19 NM_020766.2 -?/. - c.769G>C r.(?) p.(Val257Leu)


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