Variant #0000518380 (NC_000003.11:g.157823669C>G, NM_003030.4:c.145G>C (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.157823669C>G
DNA change (hg38) g.158105880C>G
Published as SHOX2(NM_001163678.1):c.145G>C (p.(Asp49His))
ISCN -
DB-ID SHOX2_000012
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 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SHOX2 NM_003030.4 -?/. - c.145G>C r.(?) p.(Asp49His)
RSRC1 NM_016625.2 -?/. - c.-4334C>G r.(?) p.(=)


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