Variant #0000861861 (NC_000010.10:g.134598798C>T, NM_177400.2:c.565G>A (NKX6-2))

Chromosome 10
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.134598798C>T
DNA change (hg38) -
Published as NKX6-2(NM_177400.3):c.565G>A (p.E189K)
ISCN -
DB-ID INPP5A_000006
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 2022-05-09 15:51:19 +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     
INPP5A NM_005539.3 ?/. - c.*3265C>T r.(=) p.(=)
NKX6-2 NM_177400.2 ?/. - c.565G>A r.(?) p.(Glu189Lys)


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