Variant #0000573841 (NC_000023.10:g.13764958T>C, OFD1(NM_003611.2):c.714T>C)

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.13764958T>C
DNA change (hg38) g.13746839T>C
Published as OFD1(NM_001330210.1):c.294T>C (p.Y98=), OFD1(NM_003611.3):c.714T>C (p.Y238=)
ISCN -
DB-ID OFD1_000002 See all 4 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) 0.00159 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAPPC2 NM_001011658.3 -/. - c.-12476A>G r.(?) p.(=)
OFD1 NM_003611.2 -/. - c.714T>C r.(?) p.(Tyr238=)