Variant #0000995357 (NC_000006.11:g.139694616A>C, NM_001168388.2:c.466T>G (CITED2))

Chromosome 6
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.139694616A>C
DNA change (hg38) -
Published as CITED2(NM_006079.4):c.466T>G (p.(Cys156Gly)), CITED2(NM_006079.5):c.466T>G (p.C156G)
ISCN -
DB-ID CITED2_000008 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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CITED2 NM_001168388.2 ?/. - c.466T>G r.(?) p.(Cys156Gly)


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