Variant #0001006391 (NC_000023.10:g.120009443C>T, NM_001242922.1:c.*2073G>A (CT47A12))

Chromosome X
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.120009443C>T
DNA change (hg38) -
Published as CT47B1(NM_001145718.1):c.82G>A (p.(Ala28Thr))
ISCN -
DB-ID CT47A12_000013
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 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     
CT47B1 NM_001145718.1 -?/. - c.82G>A r.(?) p.(Ala28Thr)
CT47A12 NM_001242922.1 -?/. - c.*2073G>A r.(=) p.(=)


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