Variant #0000273575 (NC_000016.9:g.10996577C>T, NM_000246.3:c.691C>T (CIITA))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.10996577C>T
DNA change (hg38) g.10902720C>T
Published as CIITA(NM_000246.3):c.691C>T (p.P231S), CIITA(NM_001286402.1):c.694C>T (p.P232S)
ISCN -
DB-ID CIITA_000003 See all 2 reported entries
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) 0.00179 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CIITA NM_000246.3 -/. - c.691C>T r.(?) p.(Pro231Ser)


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