Variant #0000566544 (NC_000019.9:g.17397497_17397500del, NM_152363.5:c.*136_*139del (ANKLE1))

Chromosome 19
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.17397497_17397500del
DNA change (hg38) g.17286688_17286691del
Published as ANKLE1(NM_001278443.1):c.*96_*99del (p.(=)), ANKLE1(NM_001278444.2):c.1767_1770delGTGT (p.L591Vfs*17)
ISCN -
DB-ID ANKLE1_000007 See all 2 reported entries
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKLE1 NM_152363.5 -/. - c.*136_*139del r.(=) p.(=)


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