Variant #0001055643 (NC_000016.9:g.70698189_70698203dup, NM_138383.2:c.1632_1646dup (MTSS1L))

Chromosome 16
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.70698189_70698203dup
DNA change (hg38) -
Published as MTSS2(NM_138383.3):c.1632_1646dup (p.(Gly546_Ala550dup))
ISCN -
DB-ID IL34_000009
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 2025-11-01 13:22:20 +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     
MTSS1L NM_138383.2 -?/. - c.1632_1646dup r.(?) p.(Gly546_Ala550dup)
IL34 NM_152456.2 -?/. - c.*4099_*4113dup r.(=) p.(=)


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