Variant #0000611014 (NC_000007.13:g.19156668T>C, NM_000474.3:c.277A>G (TWIST1))

Chromosome 7
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.19156668T>C
DNA change (hg38) g.19117045T>C
Published as TWIST1(NM_000474.3):c.277A>G (p.S93G, p.(Ser93Gly))
ISCN -
DB-ID TWIST1_000028 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 2019-12-04 15:24:38 +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     
TWIST1 NM_000474.3 -?/. - c.277A>G r.(?) p.(Ser93Gly)


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