Variant #0000656444 (NC_000010.10:g.127442257T>C, NC_000010.10(NM_015608.2):c.3292-6T>C (C10orf137))

Chromosome 10
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.127442257T>C
DNA change (hg38) g.125753688T>C
Published as EDRF1(NM_001202438.1):c.3394-6T>C (p.(=))
ISCN -
DB-ID C10orf137_000004
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) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-03-23 16:13:27 +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     
C10orf137 NM_015608.2 -?/. - c.3292-6T>C r.(=) p.(=)


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