Variant #0000856371 (NC_000023.10:g.13753428A>G, NM_003611.2:c.74A>G (OFD1))

Chromosome X
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.13753428A>G
DNA change (hg38) -
Published as OFD1(NM_003611.2):c.74A>G (p.Q25R), OFD1(NM_003611.3):c.74A>G (p.Q25R)
ISCN -
DB-ID OFD1_000115 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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:47:41 +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     
TRAPPC2 NM_001011658.3 ?/. - c.-946T>C r.(?) p.(=)
OFD1 NM_003611.2 ?/. - c.74A>G r.(?) p.(Gln25Arg)


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