Variant #0000536341 (NC_000009.11:g.130588091C>T, NM_000118.3:c.572G>A (ENG))

Chromosome 9
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.130588091C>T
DNA change (hg38) g.127825812C>T
Published as ENG(NM_000118.3):c.572G>A (p.G191D), ENG(NM_000118.4):c.572G>A (p.G191D), ENG(NM_001114753.2):c.572G>A (p.(Gly191Asp), p.G191D)
ISCN -
DB-ID ENG_000008 See all 7 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) 0.00874 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
ENG NM_000118.3 -?/. - c.572G>A r.(?) p.(Gly191Asp)


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