Variant #0000562478 (NC_000017.10:g.57148256A>G, NM_015294.3:c.737T>C (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.57148256A>G
DNA change (hg38) g.59070895A>G
Published as TRIM37(NM_001005207.2):c.737T>C (p.(Met246Thr))
ISCN -
DB-ID TRIM37_000051
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) 8.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM37 NM_001005207.2 -?/. - c.737T>C r.(?) p.(Met246Thr)
PPM1E NM_014906.4 -?/. - c.*89864A>G r.(=) p.(=)
TRIM37 NM_015294.3 -?/. - c.737T>C r.(?) p.(Met246Thr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.