Variant #0000692341 (NC_000017.10:g.40729692G>A, NM_170607.2:c.*6071G>A (MLX))

Chromosome 17
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.40729692G>A
DNA change (hg38) -
Published as PSMC3IP(NM_016556.3):c.13C>T (p.R5W)
ISCN -
DB-ID FAM134C_000010
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) 0.00023 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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TUBG1 NM_001070.4 ?/. - c.-32064G>A r.(?) p.(=)
PSMC3IP NM_013290.6 ?/. - c.13C>T r.(?) p.(Arg5Trp)
MLX NM_170607.2 ?/. - c.*6071G>A r.(=) p.(=)
FAM134C NM_178126.3 ?/. - c.*4139C>T r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.