Variant #0000323712 (NC_000014.8:g.61446302_61446305del, NM_001172702.1:c.-1694_-1691del (SLC38A6))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.61446302_61446305del
DNA change (hg38) g.60979584_60979587del
Published as TRMT5(NM_020810.2):c.312_315del (p.(Ile105Serfs*4))
ISCN -
DB-ID TRMT5_000002 See all 3 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_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 2022-05-09 15:51:19 +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.-1694_-1691del r.(?) p.(=)
TRMT5 NM_020810.2 +/. - c.312_315del r.(?) p.(Ile105SerfsTer4)


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