Variant #0000895187 (NC_000019.9:g.7293862A>G, NM_000208.2:c.41T>C (INSR))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7293862A>G
DNA change (hg38) -
Published as INSR(NM_000208.2):c.41T>C (p.(Leu14Pro)), INSR(NM_000208.4):c.41T>C (p.L14P)
ISCN -
DB-ID INSR_000145 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) 0.00024 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +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     
INSR NM_000208.2 -?/. - c.41T>C r.(?) p.(Leu14Pro)


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