Variant #0000322211 (NC_000011.9:g.45947773G>C, PHF21A(NM_001101802.1):c.*7746C>G)

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.45947773G>C
DNA change (hg38) g.45926222G>C
Published as GYLTL1B(NM_152312.3):c.883G>C (p.(Asp295His))
ISCN -
DB-ID GYLTL1B_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 2020-03-23 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.*7746C>G r.(=) p.(=)
GYLTL1B NM_152312.3 ?/. - c.883G>C r.(?) p.(Asp295His)