Variant #0001031013 (NC_000001.10:g.104078071G>C, NM_020978.4:c.-19867G>C (AMY2B))

Chromosome 1
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.104078071G>C
DNA change (hg38) -
Published as RNPC3(NM_017619.4):c.555+8G>C
ISCN -
DB-ID RNPC3_000016
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
RNPC3 NM_017619.3 -?/. - c.555+8G>C - r.(=) p.(=)
AMY2B NM_020978.4 -?/. - c.-19867G>C - r.(?) p.(=)


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