Transcript #00025626 (NM_001304548.1, CXorf59 gene)

Transcript name transcript variant 1
Gene name CXorf59 (chromosome X open reading frame 59)
Chromosome X
Transcript - NCBI ID NM_001304548.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001291477.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2021-06-29 21:35:15 +02:00 (CEST)
Date last edited N/A


Variants

69 entries on 1 page. Showing entries 1 - 69.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-1_6818-10658{inv} r.? p.?
+/. _1_64_ c.-66_*313{0} r.0 p.0
+/. _1_64_ c.-66_*313{0} r.0 p.0
-?/. _1_2i c.-66_518-3135[2] r.? p.?
+/. - c.0 r.0 p.0
+/. 45i c.? r.? p.?
?/. - c.10C>T r.(?) p.(Gln4Ter)
?/. - c.17G>A r.(?) p.(Gly6Asp)
?/. - c.122G>C r.(?) p.(Arg41Pro)
?/. - c.178C>T r.(?) p.(Leu60Phe)
-?/. - c.540C>T r.(?) p.(=)
?/. - c.545A>G r.(?) p.(Gln182Arg)
-?/. - c.932C>A r.(?) p.(Thr311Asn)
-?/. - c.1131T>G r.(?) p.(Ser377Arg)
?/. - c.1322A>G r.(?) p.(Glu441Gly)
?/. - c.1547T>G r.(?) p.(Phe516Cys)
?/. - c.1694C>T r.(?) p.(Ser565Leu)
-?/. - c.2188A>G r.(?) p.(Thr730Ala)
?/. - c.2609G>A r.(?) p.(Arg870Gln)
?/. - c.2630A>G r.(?) p.(Asn877Ser)
-?/. - c.2844+13del r.(=) p.(=)
?/. - c.2864T>C r.(?) p.(Leu955Ser)
-?/. - c.3027A>G r.(?) p.(Pro1009=)
?/. - c.3573G>T r.(?) p.(Leu1191Phe)
-?/. - c.4016C>T r.(?) p.(Thr1339Ile)
-?/. - c.4140T>C r.(?) p.(Thr1380=)
?/. - c.4279G>A r.(?) p.(Ala1427Thr)
-?/. - c.4340_4342del r.(?) p.(Lys1447del)
-?/. - c.4373A>T r.(?) p.(Asp1458Val)
-?/. - c.4589A>C r.(?) p.(His1530Pro)
?/. - c.4589A>C r.(?) p.(His1530Pro)
?/. - c.4589A>C r.(?) p.(His1530Pro)
-?/. - c.4659C>T r.(?) p.(Pro1553=)
?/. - c.4916+3A>G r.spl? p.?
?/. - c.5101A>G r.(?) p.(Thr1701Ala)
?/. - c.5144G>A r.(?) p.(Arg1715His)
+/. - c.5224A>G r.(?) p.(Ser1742Gly)
?/. - c.5536-441A>G r.(=) p.(=)
-?/. - c.5631G>A r.(?) p.(Val1877=)
-?/. - c.6103G>A r.(?) p.(Asp2035Asn)
-?/. - c.6180T>G r.(?) p.(Ile2060Met)
-?/. - c.6694A>T r.(?) p.(Arg2232Trp)
-?/. - c.7030G>A r.(?) p.(Asp2344Asn)
+/. - c.7154T>A r.(?) p.(Ile2385Asn)
-?/. - c.7235C>T r.(?) p.(Ser2412Leu)
?/. - c.7295C>T r.(?) p.(Thr2432Ile)
-?/. - c.7571T>C r.(?) p.(Leu2524Ser)
?/. - c.7573G>C r.(?) p.(Asp2525His)
-?/. - c.7848C>G r.(?) p.(Gly2616=)
?/. - c.8014A>G r.(?) p.(Thr2672Ala)
?/. - c.8026C>G r.(?) p.(Gln2676Glu)
-?/. - c.8062G>C r.(?) p.(Asp2688His)
-?/. - c.8062G>C r.(?) p.(Asp2688His)
?/. - c.8246C>T r.(?) p.(Thr2749Met)
?/. - c.8462A>C r.(?) p.(Lys2821Thr)
-?/. - c.8540C>T r.(?) p.(Thr2847Met)
?/. - c.8617G>A r.(?) p.(Asp2873Asn)
-?/. - c.8656A>G r.(?) p.(Ile2886Val)
+/. - c.8668C>A r.(?) p.(Pro2890Thr)
-?/. - c.8806G>A r.(?) p.(Val2936Met)
-?/. - c.8852-4del r.spl? p.?
-?/. - c.9018A>G r.(?) p.(Pro3006=)
-?/. - c.9076C>T r.(?) p.(Pro3026Ser)
?/. - c.9121G>A r.(?) p.(Asp3041Asn)
-/. - c.9121G>A r.(?) p.(Asp3041Asn)
?/. - c.9203C>T r.(?) p.(Thr3068Ile)
?/. - c.9463A>G r.(?) p.(Met3155Val)
-/. - c.9463A>G r.(?) p.(Met3155Val)
?/. - c.9491G>A r.(?) p.(Arg3164His)
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