Variant #0000321355 (NC_000001.10:g.231114561_231114563dup, NM_022786.1:c.-291_-289dup (ARV1))

Chromosome 1
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.231114561_231114563dup
DNA change (hg38) g.230978815_230978817dup
Published as TTC13(NM_001122835.2):c.34_35insGCT (p.(Cys11dup))
ISCN -
DB-ID TTC13_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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARV1 NM_022786.1 ?/. - c.-291_-289dup r.(?) p.(=)
TTC13 NM_024525.4 ?/. - c.32_34dup r.(?) p.(Cys11dup)


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