Transcript #00020108 (NM_145207.2, SPATA5 gene)

Transcript name spermatogenesis associated 5
Gene name SPATA5 (spermatogenesis associated 5)
Chromosome 4
Transcript - NCBI ID NM_145207.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_660208.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

83 entries on 1 page. Showing entries 1 - 83.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.1A>C r.(?) p.(Met1?)
+?/. - c.1A>C r.(?) p.(Met1?)
+?/. - c.1A>C r.(?) p.0?
+?/. - c.1A>C r.(?) p.(Met1?)
+?/. - c.1A>C r.(?) p.(Met1?)
+/. - c.1A>C r.(?) p.(Met1?)
+?/. - c.1A>C r.(?) p.(Met1?)
+/. 2 c.250C>T r.(?) p.(Arg84*)
?/. - c.251G>A r.(?) p.(Arg84Gln)
+?/. - c.251G>A r.(?) p.(Arg84Gln)
+/. 2 c.251G>A r.(?) p.(Arg84Gln)
+/. 2 c.251G>A r.(?) p.(Arg84Gln)
+/. - c.251G>A r.(?) p.(Arg84Gln)
+/. 2 c.269G>T r.(?) p.(Ser90Ile)
+/. 2 c.269G>T r.(?) p.(Ser90Ile)
?/. - c.277G>A r.(?) p.Gly93Arg
+/. 3 c.298G>A r.(?) p.(Ala100Thr)
+?/. 3 c.394C>T r.(?) p.(Gln132*)
?/. - c.545C>T r.(?) p.(Thr182Ile)
+?/. 5 c.554G>A r.(?) p.(Gly185Glu)
+/. 5 c.556C>T r.(?) p.(Arg186*)
+/. 5 c.556C>T r.(?) p.(Arg186*)
+?/. - c.580C>T r.(?) p.(Arg194*)
+?/. 5 c.700C>T r.(?) p.(Gln234*)
-/. - c.767T>C r.(?) p.(Ile256Thr)
-?/. - c.980C>G r.(?) p.(Ser327Cys)
+/. - c.989_991del r.(?) p.(Thr330del)
+/. - c.989_991del r.(?) p.(Thr330del)
+/. - c.989_991del r.(?) p.(Thr330del)
+/. 5 c.989_991del r.(?) p.(Thr330del)
+/. - c.989_991del r.(?) p.(Thr330del)
+?/. - c.989_991del r.(?) p.(Thr330del)
+?/. - c.989_991del r.(?) p.(Thr330del)
+/. - c.989_991del r.(?) p.(Thr330del)
+/. 5 c.989_991del r.(?) p.(Thr330del)
+/. 5 c.989_991del r.(?) p.(Thr330del)
+/. 5 c.989_991del r.(?) p.(Thr330del)
+?/. - c.1069G>C r.(?) p.(Gly357Arg)
-?/. - c.1159C>T r.(?) p.(Pro387Ser)
-?/. - c.1159C>T r.(?) p.(Pro387Ser)
+/. - c.1333C>T r.(?) p.(Arg445*)
+/. - c.1334+1G>C r.spl? p.?
+/. 8 c.1343C>T r.(?) p.(Ser448Leu)
?/. - c.1345A>G r.(?) p.(Ile449Val)
-?/. - c.1461A>G r.(?) p.(Glu487=)
?/. - c.1464A>C r.(?) p.(Val488=)
+/. 9 c.1574_1578del r.(?) p.(Asn525Thrfs*20)
+/. 9 c.1574_1578del r.(?) p.(Asn525Thrfs*20)
?/. - c.1585C>T r.(?) p.(Arg529Trp)
./. 9 c.1586G>A r.(?) p.(Arg529Gln)
+/. 9 c.1586G>A r.(?) p.(Arg529Gln)
+/. - c.1612C>T r.(?) p.(Arg538Ter)
+/. - c.1677C>A r.(?) p.(Tyr559Ter)
+/. 9 c.1677C>A r.(?) p.(Tyr559*)
?/. - c.1678G>A r.(?) p.(Val560Ile)
+/. - c.1714+1G>A r.spl? p.?
+/. - c.1714+1G>A r.spl? p.?
+/. 9i c.1714+1G>A r.spl? p.?
+/. 9i c.1714+1G>A r.spl p.?
+/. - c.1810C>T r.(?) p.(Gln604*)
?/. - c.1877G>C r.(?) p.(Trp626Ser)
+/. 11 c.1878G>C r.(?) p.(Trp626Cys)
+/. 11 c.1878G>C r.(?) p.(Trp626Cys)
+?/. - c.1883A>G r.(?) p.(Asp628Gly)
+?/. - c.1883A>G r.(?) p.(Asp628Gly)
+?/. - c.1883A>G r.(?) p.(Asp628Gly)
+/. 11 c.1883A>G r.(?) p.(Asp628Gly)
+/. 11 c.1883A>G r.(?) p.(Asp628Gly)
+/. 11 c.1883A>G r.(?) p.(Asp628Gly)
?/. - c.1964G>A r.(?) p.(Arg655Gln)
-?/. - c.1964G>A r.(?) p.(Arg655Gln)
-?/. - c.2219T>C r.(?) p.(Leu740Ser)
?/. - c.2243G>A r.(?) p.(Arg748His)
?/. - c.2340+5G>A r.spl? p.?
+/. 15 c.2351G>A r.(?) p.(Arg784Gln)
+/. 15 c.2351G>A r.(?) p.(Arg784Gln)
+/. 15 c.2362_2371del r.(?) p.(Ile788Serfs*47)
+?/. 15 c.2384C>G r.(?) p.(Pro795Arg)
+?/. - c.2389C>G r.(?) p.(Pro797Ala)
?/. - c.2453A>C r.(?) p.(Glu818Ala)
-?/. - c.2506-7A>C r.(=) p.(=)
+/. 16 c.2531C>T r.(?) p.(Ala844Val)
+/. 16 c.2531C>T r.(?) p.(Ala844Val)
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