Variant #0000573320 (NC_000023.10:g.120006597dup, NM_001242922.1:c.*4919dup (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.120006597dup
DNA change (hg38) g.120872743dup
Published as CT47B1(NM_001145718.1):c.*32-3dupC (p.(=))
ISCN -
DB-ID CT47A12_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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-21 09:37:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CT47B1 NM_001145718.1 -?/. - c.*32-3dup r.spl? p.?
CT47A12 NM_001242922.1 -?/. - c.*4919dup r.(?) p.(=)


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