Variant #0000250872 (NC_000017.10:g.57141779del, NC_000017.10(NM_015294.3):c.810-3del (TRIM37))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57141779del
DNA change (hg38) g.59064418del
Published as TRIM37(NM_001005207.2):c.810-3del (p.?), TRIM37(NM_015294.6):c.810-3delT
ISCN -
DB-ID TRIM37_000032 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.810-3del r.spl? p.?
PPM1E NM_014906.4 -/. - c.*83387del r.(?) p.(=)
TRIM37 NM_015294.3 -/. - c.810-3del r.spl? p.?


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