Variant #0000618116 (NC_000020.10:g.3732575T>C, NM_001039140.2:c.*2130A>G (C20orf27))

Chromosome 20
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.3732575T>C
DNA change (hg38) g.3751928T>C
Published as HSPA12B(NM_001197327.1):c.1820T>C (p.L607P)
ISCN -
DB-ID C20orf27_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +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     
C20orf27 NM_001039140.2 ?/. - c.*2130A>G r.(=) p.(=)
HSPA12B NM_052970.4 ?/. - c.1823T>C r.(?) p.(Leu608Pro)


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