Variant #0000930833 (NC_000017.10:g.57058177C>T, NM_015294.3:c.*18561G>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.57058177C>T
DNA change (hg38) -
Published as PPM1E(NM_014906.4):c.2053C>T (p.(Pro685Ser))
ISCN -
DB-ID TRIM37_000072
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) 0.00332 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 2023-07-07 10:10:56 +02:00 (CEST)
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.*2102G>A r.(=) p.(=)
PPM1E NM_014906.4 -?/. - c.2053C>T r.(?) p.(Pro685Ser)
TRIM37 NM_015294.3 -?/. - c.*18561G>A r.(=) p.(=)


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