Variant #0000322255 (NC_000011.9:g.60899393G>T, NM_014207.3:c.*5636G>T (CD5))

Chromosome 11
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.60899393G>T
DNA change (hg38) g.61131921G>T
Published as VPS37C(NM_017966.4):c.967C>A (p.(Gln323Lys))
ISCN -
DB-ID VPS37C_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) 0.00011 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD5 NM_014207.3 ?/. - c.*5636G>T r.(=) p.(=)
VPS37C NM_017966.4 ?/. - c.967C>A r.(?) p.(Gln323Lys)


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