Variant #0000970799 (NC_000023.10:g.13778612C>G, NM_003611.2:c.2033C>G (OFD1))

Chromosome X
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.13778612C>G
DNA change (hg38) -
Published as OFD1(NM_001330210.1):c.1613C>G (p.A538G), OFD1(NM_001330210.2):c.1613C>G (p.A538G), OFD1(NM_003611.3):c.2033C>G (p.A678G)
ISCN -
DB-ID OFD1_000091 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) 0.00064 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 2024-02-26 20:06:56 +01:00 (CET)
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.-26130G>C r.(?) p.(=)
OFD1 NM_003611.2 -?/. - c.2033C>G r.(?) p.(Ala678Gly)


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