Variant #0000978484 (NC_000009.11:g.136220584C>T, NC_000009.11(NM_003172.3):c.515+20G>A (SURF1))

Chromosome 9
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.136220584C>T
DNA change (hg38) -
Published as SURF1(NM_003172.4):c.515+20G>A
ISCN -
DB-ID RPL7A_000029
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 2024-04-19 20:27:30 +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     
RPL7A NM_000972.2 -?/. - c.*2363C>T r.(=) p.(=)
SURF1 NM_003172.3 -?/. - c.515+20G>A r.(=) p.(=)


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