Variant #0000922906 (NC_000001.10:g.104076462C>T, NM_020978.4:c.-21476C>T (AMY2B))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.104076462C>T
DNA change (hg38) -
Published as RNPC3(NM_017619.4):c.342C>T (p.G114=)
ISCN -
DB-ID RNPC3_000011
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
RNPC3 NM_017619.3 -/. - c.342C>T - r.(?) p.(Gly114=)
AMY2B NM_020978.4 -/. - c.-21476C>T - r.(?) p.(=)


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