Variant #0000308480 (NC_000003.11:g.11058903G>A, NM_003042.3:c.6G>A (SLC6A1))

Chromosome 3
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.11058903G>A
DNA change (hg38) g.11017217G>A
Published as SLC6A1(NM_003042.3):c.6G>A (p.A2=), SLC6A1(NM_003042.4):c.6G>A (p.A2=)
ISCN -
DB-ID SLC6A1_000005 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) 0.00077 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC6A1 NM_003042.3 -?/. - c.6G>A r.(?) p.(Ala2=)
SLC6A1-AS1 NR_046647.1 -?/. - n.105+1903C>T r.(?) -


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