Variant #0000568752 (NC_000019.9:g.7184669_7184672dup, NC_000019.9(NM_000208.2):c.653-7_653-4dup (INSR))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7184669_7184672dup
DNA change (hg38) g.7184658_7184661dup
Published as INSR(NM_000208.2):c.653-4_653-3insTCTC (p.?), INSR(NM_000208.3):c.653-7_653-4dupTCTC
ISCN -
DB-ID INSR_000066 See all 2 reported entries
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INSR NM_000208.2 -/. - c.653-7_653-4dup r.spl? p.?


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