Variant #0000562459 (NC_000017.10:g.57093035C>T, NM_015294.3:c.2512G>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.57093035C>T
DNA change (hg38) g.59015674C>T
Published as TRIM37(NM_001005207.2):c.2512G>A (p.(Val838Ile))
ISCN -
DB-ID TRIM37_000025
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) 0.00282 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM37 NM_001005207.2 -?/. - c.2512G>A r.(?) p.(Val838Ile)
PPM1E NM_014906.4 -?/. - c.*34643C>T r.(=) p.(=)
TRIM37 NM_015294.3 -?/. - c.2512G>A r.(?) p.(Val838Ile)


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