Variant #0000973930 (NC_000001.10:g.38269983C>T, NM_198446.2:c.-4094C>T (C1orf122))

Chromosome 1
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.38269983C>T
DNA change (hg38) -
Published as YRDC(NM_024640.4):c.758G>A (p.(Arg253His))
ISCN -
DB-ID C1orf122_000007
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) 4.0E-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 2024-04-19 20:20:39 +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     
MANEAL NM_001031740.2 ?/. - c.*4452C>T r.(=) p.(=)
YRDC NM_024640.3 ?/. - c.758G>A r.(?) p.(Arg253His)
C1orf122 NM_198446.2 ?/. - c.-4094C>T r.(?) p.(=)


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