Transcript #00007376

Transcript name transcript variant 2
Gene name HCCS (holocytochrome c synthase)
Chromosome X
Transcript - NCBI ID NM_001122608.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001116080.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

28 entries on 1 page. Showing entries 1 - 28.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.5G>A r.(?) p.(Gly2Asp)
?/? c.49G>T r.(?) p.(Ala17Ser)
?/? c.78G>A r.(=) p.(=)
?/? c.100+8G>A r.(=) p.(=)
?/? c.100+9C>T r.(=) p.(=)
?/? c.100+30A>G r.(=) p.(=)
?/? c.101-11G>C r.(=) p.(=)
?/? c.176G>A r.(?) p.(Arg59His)
?/? c.177C>T r.(=) p.(=)
?/? c.189C>T r.(=) p.(=)
?/? c.215C>T r.(?) p.(Ala72Val)
?/? c.216G>C r.(=) p.(=)
?/? c.244T>C r.(?) p.(Ser82Pro)
?/? c.252+23T>C r.(=) p.(=)
?/? c.252+48C>T r.(=) p.(=)
?/? c.274C>A r.(?) p.(Pro92Thr)
?/? c.316G>C r.(?) p.(Glu106Gln)
?/? c.474C>T r.(=) p.(=)
?/? c.521C>T r.(?) p.(Ala174Val)
?/? c.521+7A>G r.(=) p.(=)
?/? c.521+33C>A r.(=) p.(=)
?/? c.522-45A>G r.(=) p.(=)
?/? c.573_574insTAT r.(?) p.(Tyr192dup)
?/? c.732C>T r.(=) p.(=)
?/? c.763G>A r.(?) p.(Val255Ile)
?/? c.794G>A r.(?) p.(Arg265His)
?/? c.*17_*18insA r.(=) p.(=)
?/? c.*26A>G r.(=) p.(=)
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