Variant #0000308873 (NC_000009.11:g.136219564G>C, NM_003172.3:c.573C>G (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.136219564G>C
DNA change (hg38) g.133352709G>C
Published as SURF1(NM_003172.4):c.573C>G (p.T191=)
ISCN -
DB-ID SURF1_000028 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) 0.03882 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.*1343G>C r.(=) p.(=)
SURF1 NM_003172.3 -/. - c.573C>G r.(?) p.(Thr191=)
SURF2 NM_017503.3 -/. - c.-3905G>C r.(?) p.(=)
MED22 NM_133640.3 -/. - c.-4826C>G r.(?) p.(=)


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