Variant #0000523897 (NC_000005.9:g.1209038_1209076del, NC_000005.9(NM_001003841.2):c.343+37_343+75del (SLC6A19))

Chromosome 5
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.1209038_1209076del
DNA change (hg38) g.1208923_1208961del
Published as SLC6A19(NM_001003841.3):c.343+37_343+75del
ISCN -
DB-ID SLC6A19_000027
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC6A19 NM_001003841.2 -?/. - c.343+37_343+75del r.(=) p.(=)


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