Variant #0000949217 (NC_000009.11:g.136220661_136220663del, NM_003172.3:c.462_464del (SURF1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.136220661_136220663del
DNA change (hg38) -
Published as SURF1(NM_003172.4):c.462_464delCTC (p.S155del)
ISCN -
DB-ID RPL7A_000028
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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL7A NM_000972.2 ?/. - c.*2440_*2442del r.(=) p.(=)
SURF1 NM_003172.3 ?/. - c.462_464del r.(?) p.(Ser155del)


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