Variant #0000978966 (NC_000010.10:g.134599446T>A, NM_177400.2:c.7A>T (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.134599446T>A
DNA change (hg38) -
Published as NKX6-2(NM_177400.3):c.7A>T (p.(Thr3Ser))
ISCN -
DB-ID INPP5A_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.*3913T>A r.(=) p.(=)
NKX6-2 NM_177400.2 ?/. - c.7A>T r.(?) p.(Thr3Ser)


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