Variant #0000287976 (NC_000023.10:g.48337450C>G, NM_012280.2:c.307C>G (FTSJ1))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48337450C>G
DNA change (hg38) g.48479062C>G
Published as FTSJ1(NM_001282157.1):c.-52C>G (p.(=)), FTSJ1(NM_177439.2):c.307C>G (p.Q103E)
ISCN -
DB-ID FTSJ1_000008 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) 0.00156 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FTSJ1 NM_012280.2 -/. - c.307C>G r.(?) p.(Gln103Glu)


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