Variant #0000330983 (NC_000006.11:g.34857312_34857317dup, NM_015245.2:c.133_138dup (ANKS1A))

Chromosome 6
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.34857312_34857317dup
DNA change (hg38) g.34889535_34889540dup
Published as ANKS1A(NM_015245.2):c.123_124insGGCGGC (p.(Gly41_Gly42insGlyGly))
ISCN -
DB-ID ANKS1A_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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAF11 NM_005643.3 ?/. - c.-1574_-1569dup r.(?) p.(=)
ANKS1A NM_015245.2 ?/. - c.133_138dup r.(?) p.(Gly45_Gly46dup)


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