Variant #0000929549 (NC_000009.11:g.136221678C>A, NC_000009.11(NM_003172.3):c.240+1G>T (SURF1))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.136221678C>A
DNA change (hg38) -
Published as SURF1(NM_003172.4):c.240+1G>T
ISCN -
DB-ID RPL7A_000017 See all 2 reported entries
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) 3.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
RPL7A NM_000972.2 +/. - c.*3457C>A r.(=) p.(=)
SURF1 NM_003172.3 +/. - c.240+1G>T r.spl? p.?
SURF2 NM_017503.3 +/. - c.-1791C>A r.(?) p.(=)


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