Variant #0000688273 (NC_000002.11:g.10192352_10192353del, NC_000002.11(NM_003597.4):c.1259-2_1259-1del (KLF11))

Chromosome 2
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.10192352_10192353del
DNA change (hg38) -
Published as KLF11(NM_001177718.1):c.1208-2_1208-1delAG
ISCN -
DB-ID CYS1_000003
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) 3.0E-5 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CYS1 NM_001037160.2 ?/. - c.*6627_*6628del r.(=) p.(=)
KLF11 NM_003597.4 ?/. - c.1259-2_1259-1del r.spl? p.?


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