Variant #0000692892 (NC_000019.9:g.55877505G>A, NM_000641.3:c.470C>T (IL11))

Chromosome 19
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.55877505G>A
DNA change (hg38) -
Published as IL11(NM_000641.4):c.470C>T (p.P157L)
ISCN -
DB-ID FAM71E2_000009
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) 0.00021 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL11 NM_000641.3 ?/. - c.470C>T r.(?) p.(Pro157Leu)
FAM71E2 NM_001145402.1 ?/. - c.-3071C>T r.(?) p.(=)


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