Variant #0000321888 (NC_000011.9:g.801631dup, NM_001191060.1:c.-4183dup (SLC25A22))

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.801631dup
DNA change (hg38) g.801631dup
Published as PIDD(NM_145886.3):c.1303-7_1303-6insA (p.(=))
ISCN -
DB-ID PIDD_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     
SLC25A22 NM_001191060.1 ?/. - c.-4183dup r.(?) p.(=)
PIDD NM_145886.3 ?/. - c.1303-7dup r.(=) p.(=)


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