Variant #0000550052 (NC_000013.10:g.24465958C>T, NM_005932.3:c.-2499G>A (MIPEP))

Chromosome 13
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.24465958C>T
DNA change (hg38) g.23891819C>T
Published as C1QTNF9B(NM_001007537.2):c.472G>A (p.(Gly158Arg))
ISCN -
DB-ID MIPEP_000009
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1QTNF9B NM_001007537.1 ?/. - c.472G>A r.(?) p.(Gly158Arg)
MIPEP NM_005932.3 ?/. - c.-2499G>A r.(?) p.(=)


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