Variant #0000543960 (NC_000011.9:g.45946349C>T, PHF21A(NM_001101802.1):c.*9170G>A)

Chromosome 11
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.45946349C>T
DNA change (hg38) g.45924798C>T
Published as LARGE2(NM_152312.4):c.678C>T (p.I226=)
ISCN -
DB-ID GYLTL1B_000014
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-30 13:16:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHF21A NM_001101802.1 -?/. - c.*9170G>A r.(=) p.(=)
GYLTL1B NM_152312.3 -?/. - c.678C>T r.(?) p.(Ile226=)