Variant #0000308874 (NC_000009.11:g.136218903G>A, NC_000009.11(NM_003172.3):c.833+13C>T (SURF1))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.136218903G>A
DNA change (hg38) g.133352048G>A
Published as SURF1(NM_003172.4):c.833+13C>T
ISCN -
DB-ID SURF1_000023
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) 5.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL7A NM_000972.2 -/. - c.*682G>A r.(=) p.(=)
SURF1 NM_003172.3 -/. - c.833+13C>T r.(=) p.(=)
SURF2 NM_017503.3 -/. - c.-4566G>A r.(?) p.(=)
MED22 NM_133640.3 -/. - c.-4165C>T r.(?) p.(=)


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