Variant #0000624173 (NC_000020.10:g.55943867A>G, NM_001190472.1:c.-9772T>C (MTRNR2L3))

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.55943867A>G
DNA change (hg38) g.57368811A>G
Published as RAE1(NM_001015885.1):c.641A>G (p.Q214R)
ISCN -
DB-ID MTRNR2L3_000001
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 2019-12-06 12:43:26 +01:00 (CET)
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     
RAE1 NM_001015885.1 ?/. - c.641A>G r.(?) p.(Gln214Arg)
MTRNR2L3 NM_001190472.1 ?/. - c.-9772T>C r.(?) p.(=)


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