Variant #0000320495 (NC_000001.10:g.6111682C>T, NM_015102.4:c.-59417G>A (NPHP4))

Chromosome 1
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.6111682C>T
DNA change (hg38) g.6051622C>T
Published as KCNAB2(NM_001199862.1):c.86C>T (p.(Thr29Met))
ISCN -
DB-ID KCNAB2_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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KCNAB2 NM_003636.3 ?/. - c.119+9750C>T r.(=) p.(=)
NPHP4 NM_015102.4 ?/. - c.-59417G>A r.(?) p.(=)


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