Sentence examples for variants were absent from inspiring English sources

Six behavior variants were absent from the majority of sites, but clearly present at one or two, although not to the extent of being habitual or customary (band B, Table S2).

All four variants were absent from 1100 ethnically matched controls.

Four of the randomly selected variants were absent in both parents, representing likely germline mutations.

The other two variants were absent in controls, but did not segregate with disease within the respective pedigrees.

More than half of the variants (3831 out of 6221) were observed only once and, of those, 3091 variants were absent in the 1000 Genomes and ESP databases.

Two novel MIR183 variants, miR-183 +3G>T) miR-183 +3G>T27C>T), were detected, eand in one proband: both were located outside the miR-183 -27C>Tequence miR-183 -27C>Ted nt residues, were absent in normal-hearing controls, but detectedseachgate winh hearing lone in the corresproband families (the variants were abotht in at least one affected relative in the corresponding family).

Restricting attention to mutations detected only once in the sequencing effort would provide a measure of rarity, but an additional requirement that the variants be absent from a pool of 7,197 X chromosomal alleles served to further exclude low-frequency neutral alleles in favor of essentially private mutations.

It has been argued that constitutively expressed variants may initially have evolved solely as replacement variants in non-cycling cells or between S-phases, when replication-dependent variants are absent.

Both KIR2DS4-normal and its' deleted variant were absent in 15% of HSPs, higher than an earlier report (3.2%) on Zambian discordant couples [ 28].

The variant was absent in 12 unaffected family members, in one with unknown phenotype and in 1200 unrelated controls [45].

The MME c.674G > C (p.G225A) missense variant was absent in our unaffected controls, but it is represented at low frequency in public control datasets (MAF = 0.02%); although the prevalence of primary headache in public datasets is unknown, this could reflect incomplete penetrance and the interaction with other genetic or environmental factors.