Variant #0000330870 (NC_000006.11:g.31380162_31380165del, NM_001177519.1:c.953_956del (MICA))

Chromosome 6
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.31380162_31380165del
DNA change (hg38) g.31412385_31412388del
Published as MICA(NM_001177519.1):c.949_952del (p.(Gly318AlafsTer67))
ISCN -
DB-ID MICA_000003
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-18 16:38:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MICA NM_001177519.1 ?/. - c.953_956del r.(?) p.(Gly318AlafsTer67)


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