Variant #0001002531 (NC_000016.9:g.70698920C>T, NM_138383.2:c.1208G>A (MTSS1L))

Chromosome 16
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.70698920C>T
DNA change (hg38) -
Published as MTSS2(NM_138383.3):c.1208G>A (p.R403Q)
ISCN -
DB-ID IL34_000005
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
MTSS1L NM_138383.2 ?/. - c.1208G>A r.(?) p.(Arg403Gln)
IL34 NM_152456.2 ?/. - c.*4830C>T r.(=) p.(=)


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