Variant #0000867137 (NC_000023.10:g.150840701_150840715del, NM_173493.2:c.1484_1498del (PASD1))

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.150840701_150840715del
DNA change (hg38) -
Published as PASD1(NM_173493.2):c.1484_1498delAGCTGCGGGAGCAGC (p.Q495_Q499del)
ISCN -
DB-ID PASD1_000072
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +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     
PASD1 NM_173493.2 ?/. - c.1484_1498del r.(?) p.(Gln495_Gln499del)


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