Variant #0000507324 (NC_000001.10:g.36786652A>G, NC_000001.10(NM_024676.4):c.1867-5A>G (SH3D21))

Chromosome 1
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.36786652A>G
DNA change (hg38) g.36321051A>G
Published as SH3D21(NM_001162530.1):c.2200-5A>G (p.?)
ISCN -
DB-ID SH3D21_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-04 11:10:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EVA1B NM_018166.1 -?/. - c.*1244T>C r.(=) p.(=)
SH3D21 NM_024676.4 -?/. - c.1867-5A>G r.spl? p.?


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