Variant #0000930882 (NC_000017.10:g.7311677_7311685dup, NM_020360.3:c.-14039_-14031dup (PLSCR3))

Chromosome 17
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.7311677_7311685dup
DNA change (hg38) -
Published as NLGN2(NM_020795.4):c.103_111dupAGCCTCGGC (p.S35_G37dup)
ISCN -
DB-ID PLSCR3_000002
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-07-07 10:10:56 +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     
TNK1 NM_003985.4 ?/. - c.*19274_*19282dup r.(=) p.(=)
PLSCR3 NM_020360.3 ?/. - c.-14039_-14031dup r.(?) p.(=)
TMEM256 NM_152766.3 ?/. - c.-4274_-4266dup r.(?) p.(=)


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