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Table 2 Predicted consequences of variants

From: Deep genome sequencing and variation analysis of 13 inbred mouse strains defines candidate phenotypic alleles, private variation and homozygous truncating mutations

  SNPs Indels Exonic SVs
Strain Synonymous Non-synonymous Stop gain/loss Frameshift variant Inframe variant Deletions Insertions
BUB/BnJ 9751 6050 44 41 169 1247 720
C57BL/10J 581 298 0 4 8 57 102
C57BR/cdJ 4400 2948 18 26 52 288 227
C58/J 5238 3362 23 35 69 330 254
DBA/1J 9782 6198 39 53 149 419 389
I/LnJ 10389 6249 42 52 150 690 1671
KK/HiJ 10816 6197 50 56 140 599 462
MOLF/EiJ 33710 17,311 108 172 439 897 1305
NZB/B1NJ 10403 6367 43 62 146 500 390
NZW/LacJ 10434 6326 46 61 146 673 425
RF/J 9891 6174 39 56 140 2033 862
SEA/GnJ 9309 6027 38 57 138 1284 614
ST/bJ 9021 5578 45 59 133 713 413