Variant #0000990417 (NC_000001.10:g.155880669C>T, NC_000001.10(NM_006912.5):c.-43-74G>A (RIT1))

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.155880669C>T
DNA change (hg38) -
Published as RIT1(NM_001256821.1):c.8G>A (p.(Arg3Lys))
ISCN -
DB-ID KIAA0907_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) 0.00014 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 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     
RIT1 NM_006912.5 ?/. - c.-43-74G>A r.(=) p.(=)
KIAA0907 NM_014949.2 ?/. - c.*3243G>A r.(=) p.(=)


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