Variant #0000302346 (NC_000002.11:g.217281158del, NC_000002.11(NM_001127207.1):c.862+128del (SMARCAL1))

Chromosome 2
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.217281158del
DNA change (hg38) g.216416435del
Published as SMARCAL1(NM_014140.3):c.862+128delC
ISCN -
DB-ID SMARCAL1_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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCAL1 NM_001127207.1 -?/. - c.862+128del r.(=) p.(=)
SMARCAL1 NM_014140.3 -?/. - c.862+128del r.(=) p.(=)


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