Variant #0000274516 (NC_000023.10:g.120008804_120008830del, NM_001242922.1:c.*2693_*2719del (CT47A12))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.120008804_120008830del
DNA change (hg38) g.120874950_120874976del
Published as CT47B1(NM_001145718.1):c.702_728delGAAGCTCACAGAGGAGGCCACAGAGGA (p.K235_E243del)
ISCN -
DB-ID CT47B1_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CT47B1 NM_001145718.1 -/. - c.702_728del r.(?) p.(Lys235_Glu243del)
CT47A12 NM_001242922.1 -/. - c.*2693_*2719del r.(=) p.(=)


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