Full data view for gene MNX1

Information The variants shown are described using the NM_001165255.1 transcript reference sequence.

20 entries on 1 page. Showing entries 1 - 20.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     

Template     

Technique     

Disease     

Reference     

Remarks     

Panel size     

Owner     
?/? c.-1304_-1303insG r.(=) p.(=) g.156803049_156803050insC Copied from the Exome Variant Server MNX1_000020 297/8414 246/5542 51/2872 - - - - - - -
?/? c.-1304_-1303insGG r.(=) p.(=) g.156803049_156803050insCC Copied from the Exome Variant Server MNX1_000019 866/8414 578/5542 288/2872 - - - - - - -
?/? c.-1272C>T r.(=) p.(=) g.156803018G>A Copied from the Exome Variant Server MNX1_000018 1/9634 1/6336 0/3298 - - - - - - -
?/? c.-1244C>A r.(=) p.(=) g.156802990G>T Copied from the Exome Variant Server MNX1_000017 1/9092 1/6030 0/3062 - - - - - - -
?/? c.-1155_-1153del r.(=) p.(=) g.156802899_156802901del Copied from the Exome Variant Server MNX1_000016 14/1212 11/896 3/316 - - - - - - -
?/? c.-783_-781del r.(=) p.(=) g.156802527_156802529del Copied from the Exome Variant Server MNX1_000015 25/1368 20/1130 5/238 - - - - - - -
?/? c.-564C>T r.(=) p.(=) g.156802310G>A Copied from the Exome Variant Server MNX1_000014 1/11746 0/7832 1/3914 - - - - - - -
?/? c.47C>A r.(?) p.(Ala16Asp) g.156801700G>T Copied from the Exome Variant Server MNX1_000013 75/4566 63/3182 12/1384 - - - - - - -
?/? c.48C>T r.(=) p.(=) g.156801699G>A Copied from the Exome Variant Server MNX1_000012 1/4566 0/3182 1/1384 - - - - - - -
?/? c.55+5C>A r.spl? p.? g.156801687G>T Copied from the Exome Variant Server MNX1_000011 33/4566 32/3182 1/1384 - - - - - - -
?/? c.56-38G>A r.(=) p.(=) g.156799371C>T Copied from the Exome Variant Server MNX1_000010 14/12570 14/8344 0/4226 - - - - - - -
?/? c.196C>G r.(?) p.(Leu66Val) g.156799193G>C Copied from the Exome Variant Server MNX1_000009 1/13002 1/8600 0/4402 - - - - - - -
?/? c.216+21C>T r.(=) p.(=) g.156799152G>A Copied from the Exome Variant Server MNX1_000008 1/12996 1/8596 0/4400 - - - - - - -
?/? c.217-46C>T r.(=) p.(=) g.156798613G>A Copied from the Exome Variant Server MNX1_000007 1/12958 1/8568 0/4390 - - - - - - -
?/? c.339G>A r.(=) p.(=) g.156798445C>T Copied from the Exome Variant Server MNX1_000006 1/12756 0/8454 1/4302 - - - - - - -
?/? c.384A>G r.(=) p.(=) g.156798400T>C Copied from the Exome Variant Server MNX1_000005 4/12624 0/8366 4/4258 - - - - - - -
?/? c.406C>T r.(=) p.(=) g.156798378G>A Copied from the Exome Variant Server MNX1_000004 2/12598 2/8348 0/4250 - - - - - - -
?/? c.430C>T r.(?) p.(Pro144Ser) g.156798354G>A Copied from the Exome Variant Server MNX1_000003 1/12678 0/8404 1/4274 - - - - - - -
?/? c.442G>A r.(?) p.(Glu148Lys) g.156798342C>T Copied from the Exome Variant Server MNX1_000002 1/12656 0/8390 1/4266 - - - - - - -
?/? c.450_455del r.(?) p.(Glu150_Asp151del) g.156798329_156798334del Copied from the Exome Variant Server MNX1_000001 16/11732 8/7752 8/3980 - - - - - - -
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