Variant #0000997477 (NC_000009.11:g.125047469T>G, NM_138777.3:c.362T>G (MRRF))

Chromosome 9
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.125047469T>G
DNA change (hg38) -
Published as MRRF(NM_138777.3):c.362T>G (p.(Val121Gly))
ISCN -
DB-ID MRRF_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
RBM18 NM_033117.3 ?/. - c.-20492A>C r.(?) p.(=)
MRRF NM_138777.3 ?/. - c.362T>G r.(?) p.(Val121Gly)


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