Variant #0000545366 (NC_000011.9:g.67068468del, NM_207354.2:c.1081del (ANKRD13D))

Chromosome 11
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.67068468del
DNA change (hg38) g.67300997del
Published as ANKRD13D(NM_207354.2):c.1081delG (p.A361Qfs*5)
ISCN -
DB-ID ANKRD13D_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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-01 09:42:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SSH3 NM_017857.3 ?/. - c.-2629del r.(?) p.(=)
ANKRD13D NM_207354.2 ?/. - c.1081del r.(?) p.(Ala361GlnfsTer5)


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