Variant #0000855762 (NC_000020.10:g.15948230G>C, NM_080676.5:c.940G>C (MACROD2))

Chromosome 20
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.15948230G>C
DNA change (hg38) -
Published as MACROD2(NM_001351661.1):c.940G>C (p.G314R)
ISCN -
DB-ID FLRT3_000007
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) 0.00079 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLRT3 NM_013281.3 -?/. - c.-1630233C>G r.(?) p.(=)
MACROD2 NM_080676.5 -?/. - c.940G>C r.(?) p.(Gly314Arg)


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