Variant #0000886913 (NC_000005.9:g.7883859T>C, NC_000005.9(NM_002454.2):c.903+469T>C (MTRR))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.7883859T>C
DNA change (hg38) -
Published as MTRR(NM_002454.3):c.903+469T>C
ISCN -
DB-ID MTRR_000069 See all 8 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-09-27 18:50:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C5orf49 NM_001089584.2 +/. - c.-32725A>G r.(?) p.(=)
MTRR NM_002454.2 +/. - c.903+469T>C r.(=) p.(=)
FASTKD3 NM_024091.3 +/. - c.-14881A>G r.(?) p.(=)


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