Variant #0000990074 (NC_000001.10:g.104080027C>T, NM_020978.4:c.-17911C>T (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.104080027C>T
DNA change (hg38) -
Published as RNPC3(NM_017619.3):c.688C>T (p.(Pro230Ser))
ISCN -
DB-ID RNPC3_000015
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 13:07:21 +02:00 (CEST)
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.688C>T - r.(?) p.(Pro230Ser)
AMY2B NM_020978.4 ?/. - c.-17911C>T - r.(?) p.(=)


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