Variant #0000810372 (NC_000023.10:g.40483167C>T, NM_144970.2:c.*6249G>A (CXorf38))

Chromosome X
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.40483167C>T
DNA change (hg38) -
Published as MPC1L(NM_001195522.2):c.350C>T (p.P117L)
ISCN -
DB-ID CXorf38_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) 8.0E-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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPC1L NM_001195522.1 ?/. - c.350C>T r.(?) p.(Pro117Leu)
CXorf38 NM_144970.2 ?/. - c.*6249G>A r.(=) p.(=)


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