Variant #0000570799 (NC_000021.8:g.45750770G>A, NM_004928.2:c.578C>T (C21orf2))

Chromosome 21
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.45750770G>A
DNA change (hg38) g.44330887G>A
Published as C21orf2(NM_001271441.1):c.575C>T (p.P192L)
ISCN -
DB-ID C21orf2_000030
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_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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PFKL NM_002626.4 ?/. - c.*4025G>A r.(=) p.(=)
C21orf2 NM_004928.2 ?/. - c.578C>T r.(?) p.(Pro193Leu)


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