Variant #0000809155 (NC_000020.10:g.10033877C>T, NM_130811.2:c.-165812C>T (SNAP25))

Chromosome 20
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.10033877C>T
DNA change (hg38) -
Published as ANKEF1(NM_022096.6):c.1988C>T (p.T663I)
ISCN -
DB-ID SNAP25_000011
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 2021-09-17 14:40:49 +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.1988C>T r.(?) p.(Thr663Ile)
SNAP25 NM_130811.2 -?/. - c.-165812C>T r.(?) p.(=)
SNAP25-AS1 NR_040710.1 -?/. - n.500-26581G>A r.(?) -


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