Transcript #00005169 (NM_198270.2, NHS gene)

Transcript name transcript variant 1
Gene name NHS (Nance-Horan syndrome (congenital cataracts and dental anomalies))
Chromosome X
Transcript - NCBI ID NM_198270.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_938011.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-29 18:22:44 +01:00 (CET)
Date last edited N/A


Variants

27 entries on 1 page. Showing entries 1 - 27.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.566-12_566-11insT 566 r.(=) p.(=) - intron 11
./. - c.1651C>T 1651 r.(?) p.(Pro551Ser) - missense -
./. - c.1651C>T 1651 r.(?) p.(Pro551Ser) - missense -
./. - c.2739A>T 2739 r.(?) p.(=) - coding-synonymous -
./. - c.3138T>C 3138 r.(?) p.(=) - coding-synonymous -
./. - c.3955T>C 3955 r.(?) p.(Phe1319Leu) - missense -
./. - c.3955T>C 3955 r.(?) p.(Phe1319Leu) - missense -
./. - c.3955T>C 3955 r.(?) p.(Phe1319Leu) - missense -
./. - c.3955T>C 3955 r.(?) p.(Phe1319Leu) - missense -
./. - c.3955T>C 3955 r.(?) p.(Phe1319Leu) - missense -
./. - c.3955T>C 3955 r.(?) p.(Phe1319Leu) - missense -
./. - c.3955T>C 3955 r.(?) p.(Phe1319Leu) - missense -
./. - c.3955T>C 3955 r.(?) p.(Phe1319Leu) - missense -
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