Variant #0000575074 (NC_000023.10:g.15841248_15841259del, AP1S2(NM_003916.3):c.*4206_*4217del)

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.15841248_15841259del
DNA change (hg38) g.15823125_15823136del
Published as ZRSR2(NM_005089.3):c.1315_1326del (p.(Arg440_Ser443del))
ISCN -
DB-ID ZRSR2_000027
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP1S2 NM_003916.3 -?/. - c.*4206_*4217del r.(=) p.(=)
ZRSR2 NM_005089.3 -?/. - c.1332_1343del r.(?) p.(Ser445_Arg448del)