Variant #0000657010 (NC_000012.11:g.123738431del, NM_152269.4:c.210del (C12orf65))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.123738431del
DNA change (hg38) g.123253884del
Published as C12orf65(NM_001194995.1):c.210delA (p.G72Afs*13), C12orf65(NM_152269.5):c.210del (p.(Gly72AlafsTer13)), MTRFR(NM_152269.5):c.210delA (p.G72Afs*13)
ISCN -
DB-ID C12orf65_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) 0.00017 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C12orf65 NM_152269.4 +/. - c.210del r.(?) p.(Gly72AlafsTer13)


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