Variant #0000333258 (NC_000023.10:g.15841254_15841259dup, AP1S2(NM_003916.3):c.*4212_*4217dup)

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.15841254_15841259dup
DNA change (hg38) g.15823131_15823136dup
Published as ZRSR2(NM_005089.3):c.1314_1315insAGCCGG (p.(Ser447_Arg448dup))
ISCN -
DB-ID ZRSR2_000016
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AP1S2 NM_003916.3 -?/. - c.*4212_*4217dup r.(=) p.(=)
ZRSR2 NM_005089.3 -?/. - c.1338_1343dup r.(?) p.(Ser447_Arg448dup)