LOVD - Variant listings for HNRNPH2

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DB-ID Hide DB-ID column Descending
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DNA change   Descending
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Var_pub_as Hide Var_pub_as column Descending
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Template Hide Template column Descending
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do not use Hide do not use column Descending
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Exon Hide Exon column Descending
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Frequency Hide Frequency column Descending
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Genetic origin Hide Genetic origin column Descending
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Protein Hide Protein column Descending
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RNA change Hide RNA change column Descending
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Variant remarks Hide Variant remarks column Descending
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Re-site Hide Re-site column Descending
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HNRNPH2_00002 c.1320C>T p.N440N DNA SEQ - - - p.=? r.(?) Tarpey 2009 recurrent, found 5 times -
HNRNPH2_00001 c.769T>A p.S257T DNA SEQ - - - p.Ser257Thr r.(?) Tarpey 2009 found once, nonrecurrent change -
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Legend: [ HNRNPH2 full legend ]
Sequence variations are described basically as recommended by the Ad-Hoc Committee for Mutation Nomenclature (AHCMN), with the recently suggested additions (den Dunnen JT and Antonarakis SE [2000], Hum.Mut. 15:7-12); for a summary see Nomenclature.
HNRNPH2 DB-ID: BD-ID = database IDentifier DNA change: Variation at DNA-level. If present, "Full Details" will show you the the full-length entry. Var_pub_as: What the variant was reported as. Template: Detection_Template do not use: do not use Exon: number of exon/intron containing variant; 2 = exon 2, 12i = intron 12, 2i_7i = exons 3 to 7, 8i_9 = border intron 8/exon 9 Frequency: Frequency if variant is non pathogenic. Genetic origin: origin of variant; unknown, germline (i.e. inherited), somatic, de novo, from parental disomy (maternal or paternal) or in vitro (cloned) when tested for functional consequences Protein: Variation at protein level. RNA change: Variation at RNA-level, (?) unknown but probably identical to DNA. Reference: Reference = reference to publication describing variant Variant remarks: Variant remarks Re-site: Variant creates (+) or destroys (-) a restriction enzyme recognition site.