Variant #0000991366 (NC_000001.10:g.6149122G>A, NM_015102.4:c.-96857C>T (NPHP4))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6149122G>A
DNA change (hg38) -
Published as KCNAB2(NM_001199862.2):c.514+11G>A
ISCN -
DB-ID KCNAB2_000011
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) 0.09392 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-08-28 13:07:21 +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     
KCNAB2 NM_003636.3 -/. - c.415+11G>A r.(=) p.(=)
NPHP4 NM_015102.4 -/. - c.-96857C>T r.(?) p.(=)


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