Variant #0000978789 (NC_000009.11:g.88661440C>T, NM_024635.3:c.*24565C>T (NAA35))

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.88661440C>T
DNA change (hg38) -
Published as GOLM1(NM_016548.4):c.412G>A (p.(Val138Ile))
ISCN -
DB-ID GOLM1_000003
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) 0.00132 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAA35 NM_024635.3 -?/. - c.*24565C>T r.(=) p.(=)
GOLM1 NM_177937.2 -?/. - c.412G>A r.(?) p.(Val138Ile)


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