Variant #0000562474 (NC_000017.10:g.57141755G>C, NM_015294.3:c.821C>G (TRIM37))

Chromosome 17
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.57141755G>C
DNA change (hg38) g.59064394G>C
Published as TRIM37(NM_015294.6):c.821C>G (p.P274R, p.(Pro274Arg))
ISCN -
DB-ID TRIM37_000048 See all 2 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_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 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM37 NM_001005207.2 ?/. - c.821C>G r.(?) p.(Pro274Arg)
PPM1E NM_014906.4 ?/. - c.*83363G>C r.(=) p.(=)
TRIM37 NM_015294.3 ?/. - c.821C>G r.(?) p.(Pro274Arg)


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