Variant #0000543958 (NC_000011.9:g.45946079A>G, NM_001101802.1:c.*9440T>C (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.45946079A>G
DNA change (hg38) g.45924528A>G
Published as GYLTL1B(NM_152312.3):c.515A>G (p.(Asn172Ser))
ISCN -
DB-ID GYLTL1B_000012
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) 0.00013 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.*9440T>C r.(=) p.(=)
GYLTL1B NM_152312.3 ?/. - c.515A>G r.(?) p.(Asn172Ser)


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