Variant #0000866377 (NC_000020.10:g.10023889G>A, NM_130811.2:c.-175800G>A (SNAP25))

Chromosome 20
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.10023889G>A
DNA change (hg38) -
Published as ANKEF1(NM_022096.6):c.466G>A (p.A156T)
ISCN -
DB-ID SNAP25_000012
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) 0.00012 View details
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     
ANKEF1 NM_022096.4 ?/. - c.466G>A r.(?) p.(Ala156Thr)
SNAP25 NM_130811.2 ?/. - c.-175800G>A r.(?) p.(=)
SNAP25-AS1 NR_040710.1 ?/. - n.500-16593C>T r.(?) -


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