Mutation Details for c.966G>A
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cDNA Name
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c.966G>A
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Exon or Intron
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exon 8
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Legacy Exon or Intron
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exon 7
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1098G/A
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Other Details
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This nucleotide change, G to A at position 1098 does not change amino acid at position 322 (V322V). This polymorphism has been detected by SSCP technique.
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Contributors
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Vouk K,
Komel R
1997-07-17
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Institute
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Medical Centre for Molecular Biology,
Institute of Biochemistry
Slovenia
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Submitted Phenotype Details
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Reference
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Vouk & Komel (NL#69)
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To check if there are any papers published about this mutation/variant on PubMed, please click here.
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