Variant #0000993335 (NC_000003.11:g.139280160C>G, NM_002899.3:c.-21600G>C (RBP1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.139280160C>G
DNA change (hg38) -
Published as NMNAT3(NM_178177.3):c.340G>C (p.(Ala114Pro))
ISCN -
DB-ID NMNAT3_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) 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NMNAT3 NM_001401600.1 -?/. - c.451G>C r.(?) p.(Ala151Pro)
RBP1 NM_002899.3 -?/. - c.-21600G>C r.(?) p.(=)
RBP2 NM_004164.2 -?/. - c.-84859G>C r.(?) p.(=)
NMNAT3 NM_178177.3 -?/. - c.340G>C r.(?) p.(Ala114Pro)


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