Variant #0000253252 (NC_000023.10:g.13774739A>G, OFD1(NM_003611.2):c.1264A>G)

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.13774739A>G
DNA change (hg38) g.13756620A>G
Published as OFD1(NM_003611.2):c.1264A>G (p.K422E), OFD1(NM_003611.3):c.1264A>G (p.K422E)
ISCN -
DB-ID OFD1_000021 See all 3 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) 0.00162 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 2022-05-09 15:24:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAPPC2 NM_001011658.3 -/. - c.-22257T>C r.(?) p.(=)
OFD1 NM_003611.2 -/. - c.1264A>G r.(?) p.(Lys422Glu)