Variant #0001050181 (NC_000001.10:g.104068822G>A, NM_020978.4:c.-29116G>A (AMY2B))

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.104068822G>A
DNA change (hg38) -
Published as RNPC3(NM_017619.4):c.130G>A (p.(Glu44Lys))
ISCN -
DB-ID RNPC3_000017
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
RNPC3 NM_017619.3 ?/. - c.130G>A - r.(?) p.(Glu44Lys)
AMY2B NM_020978.4 ?/. - c.-29116G>A - r.(?) p.(=)


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