Variant #0000332879 (NC_000009.11:g.136220621G>C, NM_003172.3:c.498C>G (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.136220621G>C
DNA change (hg38) g.133353766G>C
Published as SURF1(NM_003172.2):c.498C>G (p.(Phe166Leu))
ISCN -
DB-ID RPL7A_000008
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +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.*2400G>C r.(=) p.(=)
SURF1 NM_003172.3 ?/. - c.498C>G r.(?) p.(Phe166Leu)
SURF2 NM_017503.3 ?/. - c.-2848G>C r.(?) p.(=)


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