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Table 10 Table of pathogenic SNPs in Homo sapiens from dbSNP and covering fuzzy tandem repeats.

From: Tandem repeats discovery service (TReaDS) applied to finding novel cis-acting factors in repeat expansion diseases

Gene/Protein Seq length Num. path. SNP Covered by FTR FTR
FZD6 3806 2 0 -
NSDHL 1581 2 0 -
GJB1 1623 10 0 -
IDS 1437 5 0 -
IDS 5832 2 0 -
SLC16A2 4396 2 0 -
NSDHL 1581 2 0 -
ABCB7 2404 2 0 -
TIMM8A 1459 2 0 -
UBA1 3544 3 0 -
FLNA 8533 2 2 [1000- 3946]
MED12 6985 1 0 -
PRPS1 2156 4 0 -
ARSE 2220 4 0 -
  1. Table of pathogenic SNPs in Homo sapiens from dbSNP and covering fuzzy tandem repeats. The table reports: gene/protein code, sequence length, number of pathogenic SNP, number of pathogenic SNPs covered by FTR, FTR [Begin - End] if existing.