Variant #0000978790 (NC_000009.11:g.88692506T>C, NM_024635.3:c.*55631T>C (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.88692506T>C
DNA change (hg38) -
Published as GOLM1(NM_016548.4):c.130A>G (p.(Thr44Ala))
ISCN -
DB-ID GOLM1_000004
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) 0.0004 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.*55631T>C r.(=) p.(=)
GOLM1 NM_177937.2 -?/. - c.130A>G r.(?) p.(Thr44Ala)


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