Variant #0000624118 (NC_000020.10:g.10026226T>C, NM_130811.2:c.-173463T>C (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.10026226T>C
DNA change (hg38) g.10045578T>C
Published as ANKEF1(NM_022096.6):c.701T>C (p.L234S)
ISCN -
DB-ID SNAP25_000005
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) 0.00011 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKEF1 NM_022096.4 ?/. - c.701T>C r.(?) p.(Leu234Ser)
SNAP25 NM_130811.2 ?/. - c.-173463T>C r.(?) p.(=)
SNAP25-AS1 NR_040710.1 ?/. - n.500-18930A>G r.(?) -


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