Variant #0000690450 (NC_000009.11:g.136219374G>A, NM_003172.3:c.678C>T (SURF1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.136219374G>A
DNA change (hg38) -
Published as SURF1(NM_003172.3):c.678C>T (p.H226=)
ISCN -
DB-ID RPL7A_000020
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL7A NM_000972.2 -?/. - c.*1153G>A r.(=) p.(=)
SURF1 NM_003172.3 -?/. - c.678C>T r.(?) p.(His226=)
SURF2 NM_017503.3 -?/. - c.-4095G>A r.(?) p.(=)
MED22 NM_133640.3 -?/. - c.-4636C>T r.(?) p.(=)


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