Variant #0001001167 (NC_000014.8:g.77844153_77844156del, NM_213601.1:c.-759_-756del (TMED8))

Chromosome 14
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.77844153_77844156del
DNA change (hg38) -
Published as SAMD15(NM_001010860.1):c.392_395delAAGA (p.(Lys131fs))
ISCN -
DB-ID SAMD15_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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SAMD15 NM_001010860.1 ?/. - c.392_395del r.(?) p.(Lys131Serfs*4)
TMED8 NM_213601.1 ?/. - c.-759_-756del r.(?) p.(=)


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