Variant #0000722346 (NC_000009.11:g.136219604T>C, NM_003172.3:c.533A>G (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.136219604T>C
DNA change (hg38) -
Published as SURF1(NM_003172.4):c.533A>G (p.N178S)
ISCN -
DB-ID RPL7A_000021
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL7A NM_000972.2 ?/. - c.*1383T>C r.(=) p.(=)
SURF1 NM_003172.3 ?/. - c.533A>G r.(?) p.(Asn178Ser)
SURF2 NM_017503.3 ?/. - c.-3865T>C r.(?) p.(=)
MED22 NM_133640.3 ?/. - c.-4866A>G r.(?) p.(=)


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