Variant #0000969236 (NC_000017.10:g.7490231G>C, NM_004870.3:c.403G>C (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.7490231G>C
DNA change (hg38) -
Published as MPDU1(NM_004870.3):c.403G>C (p.(Ala135Pro))
ISCN -
DB-ID MPDU1_000016
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) 0.00419 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD68 NM_001251.2 -?/. - c.*5402G>C r.(=) p.(=)
FXR2 NM_004860.3 -?/. - c.*4917C>G r.(=) p.(=)
MPDU1 NM_004870.3 -?/. - c.403G>C r.(?) p.(Ala135Pro)
SOX15 NM_006942.1 -?/. - c.*1465C>G r.(=) p.(=)


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