Variant #0000502353 (NC_000001.10:g.104086048A>C, NM_020978.4:c.-11890A>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.104086048A>C
DNA change (hg38) g.103543426A>C
Published as RNPC3(NM_017619.3):c.1024A>C (p.(Asn342His)), RNPC3(NM_017619.4):c.1024A>C (p.N342H)
ISCN -
DB-ID RNPC3_000002 See all 2 reported entries
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) 0.00077 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +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.1024A>C - r.(?) p.(Asn342His)
AMY2B NM_020978.4 -?/. - c.-11890A>C - r.(?) p.(=)


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