Variant #0000315931 (NC_000009.11:g.136218926T>A, NM_003172.3:c.823A>T (SURF1))

Chromosome 9
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.136218926T>A
DNA change (hg38) g.133352071T>A
Published as SURF1(NM_003172.3):c.823A>T (p.I275F)
ISCN -
DB-ID SURF1_000024
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL7A NM_000972.2 ?/. - c.*705T>A r.(=) p.(=)
SURF1 NM_003172.3 ?/. - c.823A>T r.(?) p.(Ile275Phe)
SURF2 NM_017503.3 ?/. - c.-4543T>A r.(?) p.(=)
MED22 NM_133640.3 ?/. - c.-4188A>T r.(?) p.(=)


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