Variant #0000723598 (NC_000011.9:g.66050599C>T, NM_182553.2:c.292C>T (CNIH2))

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.66050599C>T
DNA change (hg38) -
Published as CNIH2(NM_182553.3):c.292C>T (p.L98F)
ISCN -
DB-ID CNIH2_000001
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YIF1A NM_020470.2 ?/. - c.*1509G>A r.(=) p.(=)
CNIH2 NM_182553.2 ?/. - c.292C>T r.(?) p.(Leu98Phe)


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