Variant #0000894062 (NC_000017.10:g.57119179G>T, NM_015294.3:c.1748C>A (TRIM37))

Chromosome 17
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.57119179G>T
DNA change (hg38) -
Published as TRIM37(NM_015294.6):c.1748C>A (p.P583H)
ISCN -
DB-ID TRIM37_000069
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) 0.00088 View details
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 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM37 NM_001005207.2 -?/. - c.1748C>A r.(?) p.(Pro583His)
PPM1E NM_014906.4 -?/. - c.*60787G>T r.(=) p.(=)
TRIM37 NM_015294.3 -?/. - c.1748C>A r.(?) p.(Pro583His)


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