Variant #0000861534 (NC_000009.11:g.136218943T>A, NM_003172.3:c.806A>T (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.136218943T>A
DNA change (hg38) -
Published as SURF1(NM_003172.3):c.806A>T (p.N269I), SURF1(NM_003172.4):c.806A>T (p.(Asn269Ile))
ISCN -
DB-ID RPL7A_000023 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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +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.*722T>A r.(=) p.(=)
SURF1 NM_003172.3 ?/. - c.806A>T r.(?) p.(Asn269Ile)


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