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MSeqDR Data Summary for the Term SLC9A6:
Ensembl Gene IDAssociated Gene NameLSDB GenesLSDB VariantsclinVar hitsEnsembl Gene IDEnsembl Transcript IDEnsembl Protein IDDescriptionChrGene StartGene EndStrandBandTranscript Start bpTranscript End bpAssociated Gene NameAssociated Transcript NameAssociated Gene DBAssociated Transcript DBTranscript countpct GC contentGene BiotypeTranscript BiotypeSource GeneSource TranscriptStatus geneStatus transcript EntrezGene IDHGNC IDHGNC SymbolRefSeq mRNASeq region id
ENSG00000269036 MSeqDR Search EnsemblSLC9A60059ENSG00000269036ENST00000595850ENSP00000470998solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6 [Source:HGNC Symbol;Acc:11079]HG1443_HG1444_PATCH1351194681351812931q26.3135119468135181168SLC9A6SLC9A6-003HGNC SymbolHGNC transcript name340.15protein_codingprotein_codingensembl_havaensembl_havaKNOWNKNOWN1047911079SLC9A60
ENSG00000198689 MSeqDR Search EnsemblSLC9A60059ENSG00000198689ENST00000370701ENSP00000359735solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6 [Source:HGNC Symbol;Acc:11079]X1350675981351294231q26.3135067598135129298SLC9A6SLC9A6-003HGNC SymbolHGNC transcript name340.15protein_codingprotein_codingensembl_havaensembl_havaKNOWNKNOWN1047911079SLC9A6NM_00117765127516

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MSeqDR Master Exome Data Set M1: 176 entries from same gene

No.ChrPositionReferenceVariantEnsemblTranscriptIDEnsemblGeneIDGene_StartGene_EndEnsemblProteinIDGenestrandUniprotcChangepChangeNaturedbSNPFreqEVSphastConsSIFTPolyphenHGMDtypesamples
1X135067680CGENST00000370695ENSG00000198689135067598135129423ENSP00000359729SLC9A61SL9A6_HUMANc.19C>Gp.R7Gnon-synNA---DAMAGINGNA-het1
2X135067680CGENST00000370698ENSG00000198689135067598135129423ENSP00000359732SLC9A61SL9A6_HUMANc.19C>Gp.R7Gnon-synNA---DAMAGINGNA-het1
3X135067686GTENST00000370695ENSG00000198689135067598135129423ENSP00000359729SLC9A61SL9A6_HUMANc.25G>Tp.A9Snon-synrs201523857---TOLERATEDNA-het3
4X135067686GTENST00000370695ENSG00000198689135067598135129423ENSP00000359729SLC9A61SL9A6_HUMANc.25G>Tp.A9Snon-synrs201523857---TOLERATEDNA-hom1
5X135067686GTENST00000370698ENSG00000198689135067598135129423ENSP00000359732SLC9A61SL9A6_HUMANc.25G>Tp.A9Snon-synrs201523857---TOLERATEDNA-het3
6X135067686GTENST00000370698ENSG00000198689135067598135129423ENSP00000359732SLC9A61SL9A6_HUMANc.25G>Tp.A9Snon-synrs201523857---TOLERATEDNA-hom1
7X135067687CGENST00000370695ENSG00000198689135067598135129423ENSP00000359729SLC9A61SL9A6_HUMANc.26C>Gp.A9Gnon-synNA---TOLERATEDNA-het1
8X135067687CGENST00000370698ENSG00000198689135067598135129423ENSP00000359732SLC9A61SL9A6_HUMANc.26C>Gp.A9Gnon-synNA---TOLERATEDNA-het1
9X135080623C+TENST00000370695ENSG00000198689135067598135129423ENSP00000359729SLC9A61SL9A6_HUMAN---18bp 3'_splice_siteNA------het853
10X135080623C+TENST00000370695ENSG00000198689135067598135129423ENSP00000359729SLC9A61SL9A6_HUMAN---18bp 3'_splice_siteNA------hom70
11X135080623C+TENST00000370698ENSG00000198689135067598135129423ENSP00000359732SLC9A61SL9A6_HUMAN---18bp 3'_splice_siteNA------het853
12X135080623C+TENST00000370698ENSG00000198689135067598135129423ENSP00000359732SLC9A61SL9A6_HUMAN---18bp 3'_splice_siteNA------hom70
13X135080623C+TENST00000370701ENSG00000198689135067598135129423ENSP00000359735SLC9A61SL9A6_HUMAN---18bp 3'_splice_siteNA------het853
14X135080623C+TENST00000370701ENSG00000198689135067598135129423ENSP00000359735SLC9A61SL9A6_HUMAN---18bp 3'_splice_siteNA------hom70
15X135080623C+TTENST00000370695ENSG00000198689135067598135129423ENSP00000359729SLC9A61SL9A6_HUMAN---18bp 3'_splice_siteNA------het46
16X135080623C+TTENST00000370698ENSG00000198689135067598135129423ENSP00000359732SLC9A61SL9A6_HUMAN---18bp 3'_splice_siteNA------het46
17X135080623C+TTENST00000370701ENSG00000198689135067598135129423ENSP00000359735SLC9A61SL9A6_HUMAN---18bp 3'_splice_siteNA------het46
18X135080667TCENST00000370695ENSG00000198689135067598135129423ENSP00000359729SLC9A61SL9A6_HUMANc.630T>Cp.S210Ssynrs1443163880.0239C=1/T=6712;C=96/T=3739;C=97/T=10451lod=377:603---het1
19X135080667TCENST00000370698ENSG00000198689135067598135129423ENSP00000359732SLC9A61SL9A6_HUMANc.534T>Cp.S178Ssynrs1443163880.0239C=1/T=6712;C=96/T=3739;C=97/T=10451lod=377:603---het1
20X135080667TCENST00000370701ENSG00000198689135067598135129423ENSP00000359735SLC9A61SL9A6_HUMANc.474T>Cp.S158Ssynrs1443163880.0239C=1/T=6712;C=96/T=3739;C=97/T=10451lod=377:603---het1
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       Transcripts and variants in the surrounding SLC9A6 X:135067598..135129423 region Gbrowse