Variant #0000329681 (NC_000003.11:g.157823583_157823591dup, NM_003030.4:c.224_232dup (SHOX2))

Chromosome 3
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.157823583_157823591dup
DNA change (hg38) g.158105794_158105802dup
Published as SHOX2(NM_001163678.1):c.224_232dup (p.(Gly75_Gly77dup))
ISCN -
DB-ID SHOX2_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SHOX2 NM_003030.4 -?/. - c.224_232dup r.(?) p.(Gly75_Gly77dup)


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