Variant #0000563160 (NC_000017.10:g.7489255T>G, NC_000017.10(NM_004870.3):c.170-9T>G (MPDU1))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7489255T>G
DNA change (hg38) g.7585937T>G
Published as MPDU1(NM_004870.3):c.170-9T>G
ISCN -
DB-ID MPDU1_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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
CD68 NM_001251.2 -?/. - c.*4426T>G r.(=) p.(=)
MPDU1 NM_004870.3 -?/. - c.170-9T>G r.(=) p.(=)
SOX15 NM_006942.1 -?/. - c.*2441A>C r.(=) p.(=)


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