Variant #0000996231 (NC_000007.13:g.139090468G>A, NM_197964.4:c.*60018G>A (C7orf55))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.139090468G>A
DNA change (hg38) -
Published as LUC7L2(NM_001244584.2):c.643G>A (p.(Val215Met))
ISCN -
DB-ID C7orf55_000001
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
C7orf55-LUC7L2 NM_001244584.2 ?/. - c.643G>A r.(?) p.(Val215Met)
LUC7L2 NM_016019.4 ?/. - c.445G>A r.(?) p.(Val149Met)
C7orf55 NM_197964.4 ?/. - c.*60018G>A r.(=) p.(=)


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