Variant #0000324596 (NC_000016.9:g.11035792_11035794dup, NM_015226.2:c.-2783_-2781dup (CLEC16A))

Chromosome 16
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.11035792_11035794dup
DNA change (hg38) g.10941935_10941937dup
Published as DEXI(NM_014015.3):c.76_77insTGC (p.?)
ISCN -
DB-ID DEXI_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_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     
DEXI NM_014015.3 ?/. - c.74_76dup r.(?) p.(Leu25dup)
CLEC16A NM_015226.2 ?/. - c.-2783_-2781dup r.(?) p.(=)


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