Variant #0000866279 (NC_000019.9:g.59022705C>T, NM_012254.2:c.618G>A (SLC27A5))

Chromosome 19
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.59022705C>T
DNA change (hg38) -
Published as SLC27A5(NM_012254.2):c.618G>A (p.P206=)
ISCN -
DB-ID SLC27A5_000007
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC27A5 NM_012254.2 -?/. - c.618G>A r.(?) p.(Pro206=)
ZBTB45 NM_032792.2 -?/. - c.*2716G>A r.(=) p.(=)


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