Variant #0000888248 (NC_000008.10:g.17132462A>G, NM_004686.4:c.*24909T>C (MTMR7))

Chromosome 8
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.17132462A>G
DNA change (hg38) -
Published as VPS37A(NM_152415.3):c.637A>G (p.I213V)
ISCN -
DB-ID MTMR7_000007
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) 0.00323 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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     
MTMR7 NM_004686.4 -/. - c.*24909T>C r.(=) p.(=)
VPS37A NM_152415.2 -/. - c.637A>G r.(?) p.(Ile213Val)


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