Variant #0000855763 (NC_000020.10:g.15967803G>A, NM_080676.5:c.1153G>A (MACROD2))

Chromosome 20
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.15967803G>A
DNA change (hg38) -
Published as MACROD2(NM_001351661.1):c.1153G>A (p.A385T)
ISCN -
DB-ID FLRT3_000008
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLRT3 NM_013281.3 ?/. - c.-1649806C>T r.(?) p.(=)
MACROD2 NM_080676.5 ?/. - c.1153G>A r.(?) p.(Ala385Thr)


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