Variant #0000543967 (NC_000011.9:g.45950260G>A, PHF21A(NM_001101802.1):c.*5259C>T)

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.45950260G>A
DNA change (hg38) g.45928709G>A
Published as GYLTL1B(NM_152312.3):c.2030G>A (p.(Arg677His))
ISCN -
DB-ID GYLTL1B_000021
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) 0.00102 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.*5259C>T r.(=) p.(=)
GYLTL1B NM_152312.3 -?/. - c.2030G>A r.(?) p.(Arg677His)