Variant #0000607478 (NC_000002.11:g.217311886G>A, NC_000002.11(NM_001127207.1):c.1851+5G>A (SMARCAL1))

Chromosome 2
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.217311886G>A
DNA change (hg38) g.216447163G>A
Published as SMARCAL1(NM_001127207.1):c.1851+5G>A (p.?), SMARCAL1(NM_014140.3):c.1851+5G>A
ISCN -
DB-ID SMARCAL1_000050 See all 3 reported entries
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) 0.00067 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCAL1 NM_001127207.1 ?/. - c.1851+5G>A r.spl? p.?
SMARCAL1 NM_014140.3 ?/. - c.1851+5G>A r.spl? p.?


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