Variant #0000726814 (NC_000018.9:g.19371386_19371387insTCTC, NM_020774.3:c.960_961insTCTC (MIB1))

Chromosome 18
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.19371386_19371387insTCTC
DNA change (hg38) -
Published as MIB1(NM_020774.3):c.960_961insTCTC (p.D321Sfs*18)
ISCN -
DB-ID MIB1_000154
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MIB1 NM_020774.3 +?/. - c.960_961insTCTC r.(?) p.(Asp321Serfs*18)


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