Variant #0000320781 (NC_000001.10:g.44476405G>T, NM_201649.3:c.399C>A (SLC6A9))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.44476405G>T
DNA change (hg38) g.44010733G>T
Published as SLC6A9(NM_001024845.2):c.180C>A (p.(Asn60Lys))
ISCN -
DB-ID SLC6A9_000002
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CCDC24 NM_152499.1 ?/. - c.*14573G>T r.(=) p.(=)
SLC6A9 NM_201649.3 ?/. - c.399C>A r.(?) p.(Asn133Lys)


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