Variant #0000561530 (NC_000017.10:g.40725656G>C, NM_170607.2:c.*2035G>C (MLX))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.40725656G>C
DNA change (hg38) g.42573638G>C
Published as PSMC3IP(NM_001256015.2):c.101-15C>G
ISCN -
DB-ID MLX_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) 0.55173 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSMC3IP NM_013290.6 -/. - c.338-51C>G r.(=) p.(=)
MLX NM_170607.2 -/. - c.*2035G>C r.(=) p.(=)


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