Variant #0000324867 (NC_000016.9:g.70721998G>C, NM_138383.2:c.-2304C>G (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.70721998G>C
DNA change (hg38) g.70688095G>C
Published as VAC14(NM_018052.3):c.2187-5C>G (p.?)
ISCN -
DB-ID VAC14_000001
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-10 12:09:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VAC14 NM_018052.3 ?/. - c.2187-5C>G r.spl? p.?
MTSS1L NM_138383.2 ?/. - c.-2304C>G r.(?) p.(=)


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