Variant #0000311621 (NC_000009.11:g.136223246_136223266del, NC_000009.11(NM_003172.3):c.54+34_55-47del (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.136223246_136223266del
DNA change (hg38) g.133356370_133356390del
Published as SURF1(NM_003172.4):c.54+34_55-47delTGCGGGGTGCGGGGTGCGGGG
ISCN -
DB-ID SURF1_000033 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +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.*5025_*5045del r.(=) p.(=)
SURF1 NM_003172.3 -/. - c.54+34_55-47del r.? p.?
SURF2 NM_017503.3 -/. - c.-223_-203del r.(?) p.(=)


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