Variant #0000922991 (NC_000001.10:g.161090298C>T, NC_000001.10(NM_001185092.1):c.717+276C>T (NIT1))

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.161090298C>T
DNA change (hg38) -
Published as NIT1(NM_001185093.1):c.682C>T (p.(Arg228Trp))
ISCN -
DB-ID DEDD_000002
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) 0.0001 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 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DEDD NM_001039711.1 ?/. - c.*1639G>A r.(=) p.(=)
NIT1 NM_001185092.1 ?/. - c.717+276C>T r.(=) p.(=)
PFDN2 NM_012394.3 ?/. - c.-2482G>A r.(?) p.(=)


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