Variant #0000657458 (NC_000014.8:g.61446625dup, NM_001172702.1:c.-1371dup (SLC38A6))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61446625dup
DNA change (hg38) g.60979907dup
Published as TRMT5(NM_001350253.1):c.96-4dupT
ISCN -
DB-ID SLC38A6_000002 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-07-05 15:05:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC38A6 NM_001172702.1 -/. - c.-1371dup r.(?) p.(=)
TRMT5 NM_020810.2 -/. - c.12-4dup r.spl? p.?


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