Variant #0000543966 (NC_000011.9:g.45950254G>A, NM_001101802.1:c.*5265C>T (PHF21A))

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.45950254G>A
DNA change (hg38) g.45928703G>A
Published as GYLTL1B(NM_152312.3):c.2024G>A (p.(Arg675His))
ISCN -
DB-ID GYLTL1B_000020
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) 4.0E-5 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHF21A NM_001101802.1 ?/. - c.*5265C>T r.(=) p.(=)
GYLTL1B NM_152312.3 ?/. - c.2024G>A r.(?) p.(Arg675His)


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