Variant #0000914204 (NC_000014.8:g.61113278T>A, NM_005982.3:c.578A>T (SIX1))

Chromosome 14
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.61113278T>A
DNA change (hg38) -
Published as SIX1(NM_005982.3):c.578A>T (p.N193I, p.(Asn193Ile)), SIX1(NM_005982.4):c.578A>T (p.N193I)
ISCN -
DB-ID SIX1_000001 See all 4 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) 0.00036 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SIX1 NM_005982.3 -?/. - c.578A>T r.(?) p.(Asn193Ile)


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