Variant #0000611950 (NC_000009.11:g.136219623T>C, NC_000009.11(NM_003172.3):c.516-2A>G (SURF1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.136219623T>C
DNA change (hg38) g.133352768T>C
Published as -
ISCN -
DB-ID SURF1_000008 See all 3 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) 2.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +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.*1402T>C r.(=) p.(=)
SURF1 NM_003172.3 +?/. - c.516-2A>G r.spl? p.?
SURF2 NM_017503.3 +?/. - c.-3846T>C r.(?) p.(=)
MED22 NM_133640.3 +?/. - c.-4885A>G r.(?) p.(=)


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