Variant #0000325064 (NC_000016.9:g.89724282G>T, NM_002768.3:c.-286C>A (CHMP1A))

Chromosome 16
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.89724282G>T
DNA change (hg38) g.89657874G>T
Published as SPATA33(NM_001271907.1):c.-38G>T (p.(=))
ISCN -
DB-ID C16orf55_000001
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) 9.0E-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 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     
CHMP1A NM_002768.3 ?/. - c.-286C>A r.(?) p.(=)
C16orf55 NM_153025.1 ?/. - c.34+39G>T r.(=) p.(=)


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