Variant #0000308436 (NC_000017.10:g.79219954G>A, NM_001086521.1:c.*5138G>A (C17orf89))

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.79219954G>A
DNA change (hg38) g.81246154G>A
Published as SLC38A10(NM_001037984.3):c.2762C>T (p.T921M)
ISCN -
DB-ID SLC38A10_000001
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) 3.0E-5 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 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     
C17orf89 NM_001086521.1 -?/. - c.*5138G>A r.(=) p.(=)
SLC38A10 NM_138570.2 -?/. - c.*5061C>T r.(=) p.(=)


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