Variant #0000721206 (NC_000007.13:g.117351727_117351728del, NM_033427.2:c.4856_4857del (CTTNBP2))

Chromosome 7
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.117351727_117351728del
DNA change (hg38) -
Published as CTTNBP2(NM_001363349.1):c.4802_4803delAA (p.K1601Sfs*16)
ISCN -
DB-ID CTTNBP2_000019
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTTNBP2 NM_033427.2 ?/. - c.4856_4857del r.(?) p.(Lys1619Serfs*16)


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