Variant #0000925576 (NC_000012.11:g.123741386G>A, NM_152269.4:c.309G>A (C12orf65))

Chromosome 12
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.123741386G>A
DNA change (hg38) -
Published as MTRFR(NM_001194995.1):c.309G>A (p.Q103=)
ISCN -
DB-ID C12orf65_000015
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) 0.00167 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 2023-04-16 21:50:28 +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     
CDK2AP1 NM_004642.3 -?/. - c.*4897C>T r.(=) p.(=)
C12orf65 NM_152269.4 -?/. - c.309G>A r.(?) p.(Gln103=)


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