Variant #0000569121 (NC_000020.10:g.14307828A>C, NC_000020.10(NM_080676.5):c.272-166297A>C (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.14307828A>C
DNA change (hg38) g.14327182A>C
Published as FLRT3(NM_198391.2):c.325T>G (p.L109V)
ISCN -
DB-ID FLRT3_000003
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) 0.00011 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FLRT3 NM_013281.3 ?/. - c.325T>G r.(?) p.(Leu109Val)
MACROD2 NM_080676.5 ?/. - c.272-166297A>C r.(=) p.(=)


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