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Table 2 De novo variance in children with SPD

From: Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction

  PolyPhen2 HVAR score Mutation type AA position AA change Chromosome position Base change
MBD5 Stop 318 S- > Stop 149,226,465 TCA - > TAA
FMN2 .86 Missense 947 P- > L 240,370,952 CCT - > CTT
DNAH9 .88 Missense 2716 R- > W 11,696,904 CGG - > TGG
KLHL33 .96 Missense 263 R- > W 20,898,048 CGG - > TGG
PFDN6 .99 Missense 62 P- > L 33,258,152 CCG - > CTG
SLCO2B1 1.0 Missense 651 L- > P 74,915,513 CTG - > CCG
MCM2 0 Missense 636 P- > L 127,337,968 CCG - > CTG
TULP4 .06 Missense 1456 G- > R 158,925,061 GGG - > AGG
SPTYD1 .003 Missense 135 N- > S 18,637,417 AAT - > AGT
  1. AA Amino acid, S Serine, P Proline, L Leucine, R Arginine, W Tryptophan, G Glycine, N Asparagine