Variant #0000324400 (NC_000016.9:g.1034730A>C, NM_022773.2:c.-13750T>G (LMF1))

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.1034730A>C
DNA change (hg38) g.984730A>C
Published as SOX8(NM_014587.3):c.685A>C (p.(Thr229Pro)), SOX8(NM_014587.4):c.685A>C (p.T229P)
ISCN -
DB-ID SOX8_000002 See all 2 reported entries
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOX8 NM_014587.3 ?/. - c.685A>C r.(?) p.(Thr229Pro)
LMF1 NM_022773.2 ?/. - c.-13750T>G r.(?) p.(=)


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