Transcript #00020015 (NM_001012415.2, SOHLH1 gene)

Transcript name transcript variant 2
Gene name SOHLH1 (spermatogenesis and oogenesis specific basic helix-loop-helix 1)
Chromosome 9
Transcript - NCBI ID NM_001012415.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001012415.2
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

45 entries on 1 page. Showing entries 1 - 45.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-2978G>A r.(?) p.(=)
-?/. - c.-2939G>A r.(?) p.(=)
-?/. - c.-2890T>C r.(?) p.(=)
-?/. - c.-2890T>C r.(?) p.(=)
?/. - c.-2864G>A r.(?) p.(=)
-?/. - c.-2850C>G r.(?) p.(=)
-?/. - c.-2849C>T r.(?) p.(=)
?/. - c.-2841G>A r.(?) p.(=)
-/. - c.-2821C>T r.(?) p.(=)
-/. - c.-2821C>T r.(?) p.(=)
?/. - c.1A>G r.(?) p.(Met1?)
+/. - c.27C>G r.(?) p.(Tyr9*)
-/. - c.48T>C r.(?) p.(Pro16=)
-/. - c.48T>C r.(?) p.(Pro16=)
-/. - c.65+19G>A r.(?) p.(=)
-/. - c.65+19G>A r.(?) p.(=)
?/. - c.66-8C>T r.(=) p.(=)
-/. - c.91T>C r.(?) p.(Cys31Arg)
-/. - c.110A>G r.(?) p.(Gln37Arg)
-/. - c.110A>G r.(?) p.(Gln37Arg)
-/. - c.198-25G>A r.(?) p.(=)
-/. - c.198-25G>A r.(?) p.(=)
-?/. - c.210G>A r.(?) p.(=)
?/. - c.272C>T r.(?) p.(Ala91Val)
-/. - c.345+37A>G r.(?) p.(=)
-/. - c.345+37A>G r.(?) p.(=)
+?/. - c.346-1G>A r.spl p.?
+?/. - c.346-1G>A r.spl p.?
+?/. 3i c.346-1G>T r.(346_363del) p.(Ile116_Ly121del)
+?/. 3i c.346-1G>T r.(346_363del) p.(Ile116_Ly121del)
-?/. - c.404C>T r.(?) p.(Thr135Met)
-?/. - c.467+41C>T r.(?) p.(=)
-?/. - c.529C>A r.(?) p.(Pro177Thr)
-?/. - c.537C>T r.(?) p.(Pro179=)
+/. - c.705del r.(?) p.(Lys236Argfs*3)
+/. - c.705del r.(?) p.(Lys236Argfs*3)
-/. - c.804G>T r.(?) p.(Gly268=)
-/. - c.805C>T r.(?) p.(Pro269Ser)
-/. - c.875+42G>A r.(?) p.(=)
-/. - c.876-6T>C r.(?) p.(=)
-/. - c.876-6T>C r.(?) p.(=)
-/. - c.981C>T r.(?) p.(Pro327=)
-/. - c.981C>T r.(?) p.(Pro327=)
-?/. - c.*575A>G r.(=) p.(=)
-?/. - c.*688G>C r.(=) p.(=)
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