Variant #0000560634 (NC_000017.10:g.18881605C>A, NC_000017.10(NM_152351.4):c.982+1303C>A (SLC5A10))

Chromosome 17
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.18881605C>A
DNA change (hg38) g.18978292C>A
Published as FAM83G(NM_001039999.2):c.1374G>T (p.(Gln458His))
ISCN -
DB-ID FAM83G_000005
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) 0.00561 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 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     
FAM83G NM_001039999.2 -?/. - c.1374G>T r.(?) p.(Gln458His)
GRAP NM_006613.3 -?/. - c.*43667G>T r.(=) p.(=)
SLC5A10 NM_152351.4 -?/. - c.982+1303C>A r.(=) p.(=)


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