Variant #0000573740 (NC_000023.10:g.135326925_135326928del, NM_024597.3:c.289_292del (MAP7D3))

Chromosome X
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.135326925_135326928del
DNA change (hg38) g.136244766_136244769del
Published as MAP7D3(NM_001173517.1):c.289_292delAAGA (p.K97Pfs*16)
ISCN -
DB-ID MAP7D3_000037
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 2020-07-21 10:12:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP7D3 NM_024597.3 ?/. - c.289_292del r.(?) p.(Lys97ProfsTer16)


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